Chemistry:Hydroxylamine-O-sulfonic acid

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Hydroxylamine-O-sulfonic acid
H3NOSO3.png
HOSAimproved.jpg
Names
Other names
Aminosulfuric acid
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 220-971-6
Properties
H3NO4S
Molar mass 113.09
Appearance white solid
Melting point 210 °C
cold water
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

Hydroxylamine-O-sulfonic acid (HOSA) or aminosulfuric acid is the inorganic compound with molecular formula H3NO4S that is formed by the sulfonation of hydroxylamine with oleum.[1] It is a white, water-soluble and hygroscopic, solid, commonly represented by the condensed structural formula H2NOSO3H, though it actually exists as a zwitterion[2] and thus is more accurately represented as +H3NOSO3−. It is used as a reagent for the introduction of amine groups (–NH2), for the conversion of aldehydes into nitriles and alicyclic ketones into lactams (cyclic amides), and for the synthesis of variety of nitrogen-containing heterocycles.[2][3][4]

Preparation

According to a laboratory procedure[1] hydroxylamine-O-sulfonic acid can be prepared by treating hydroxylamine sulfate with fuming sulfuric acid (oleum). The industrial process is similar.[5]

(NH3OH)2SO4 + 2SO3 → 2H2NOSO3H + H2SO4

The sulfonation of hydroxylamine can also be effected with chlorosulfonic acid[2] by a method first published in 1925[6] and refined for Organic Syntheses.[7]

Structure

Analogous to sulfamic acid (H3N+SO3−) and as is the case generally for amino acids, HOSA exists in the solid state as a zwitterion: H3N+OSO3−. It resembles an ammonia molecule coordinate covalently bonded to a sulfate group.[8]

Reactions

HOSA reacts under basic conditions as nucleophile and under neutral and acid conditions as electrophile.[3][9]

Reaktivität of Hydroxylamine-O-sulfonsäure als Elektrophil und als Nukleophil

Aminations

Synthesis of N-Aminopiperidin with HOSA

It reacts with tertiary amines to trisubstituted hydrazinium salts and with pyridine to the 1-amino pyridinium salt.[10]

Synthesis of 1-Aminopyridin with HOSA

From 1-aminopyridinium salts the photochemically active 1-N-iminopyridinium ylides are accessible by acylation.[11] The photochemical rearrangement of the obtained 1-N-iminipyridinium ylides leads in high yields to 1H-1,2-diazepines[12]

Synthesis of 1,2-Diazepinen aus Iminopyridiniumyliden

N-amination of 1H-benzotriazole with hydroxylamine-O-sulfonic acid yields a mixture of 1-aminobenzotriazole (major product) and 2-aminobenzotriazole (minor product). From 1-aminotriazole, benzyne is formed in an almost quantitative yield by oxidation with lead(IV) acetate, which rapidly dimerizes to biphenylene in good yields.[13]

Synthesis of Benzyne and Biphenylene from 1-Aminobenzotriazole

Electron deficient heterocycles, such as tetrazole, can be N-aminated with hydroxylamine-O-sulfonic acid, while even more electron-deficient compounds, such as 5-nitrotetrazole, react only with stronger aminating agents such as O-tosylhydroxylamine or O- mesitylene sulfonylhydroxylamine to amino compounds, which were investigated as explosives.[14]

1-Aminotetrazol und 2-Aminotetrazol durch Aminierung of Tetrazol with HOSA

In the N-amination of the unsubstituted tetrazole, a mixture of 1-amino- and 2-aminotetrazole is obtained.

Synthesis of Sulfiminen with HOSA

Also sulfur compounds (such as thioethers) can be aminated with hydroxylamine-O-sulfonic acid to sulfinimines (isosteric with sulfoxides but far more unstable) or phosphorus compounds (such as triphenylphosphine) can be aminated to phosphine imides via the intermediate aminotriphenylphosphonium hydrogen sulfate.[15]

Phosphinimine.svg

The reaction of hydroxylamine-O-sulfonic acid with metal salts of sulfinic acids in sodium acetate solution produces primary sulfonamides in very good yields.[16]

Synthesis of primären Sulfonamiden aus Sulfinaten

Diimine can formed in situ from hydroxylamine-O-sulfonic acid respectively hydroxylamine-O-sulfonic acid hydroxylamine sulfate mixtures, which hydrogenates selectively conjugated multiple bonds.[20]

With carbonyl compounds

At room temperature and below, hydroxylamine-O-sulfonic acid reacts with ketones and aldehydes as a nucleophile to the corresponding oxime-O-sulfonic acids or their salts.[17] The oxime-O-sulfonic acids of aldehydes react above room temperature upon elimination of sulfuric acid in high yields to nitriles.[18]

Reaktion of HOSA with Carbonylverbindungen

Aliphatic ketones provide under similar conditions in very high yields oximes, arylalkyl ketones react in a Beckmann rearrangement to amides. When heated to reflux for several hours under acidic conditions (e.g., in the presence of concentrated formic acid) alicyclic ketones react to provide lactams in high yields.[19]

2-Azacyclooctanon durch Reaktion of Cycloheptanon with HOSA

Under basic conditions in the presence of primary amines, hydroxylamine-O-sulfonic acid forms with aldehydes and ketones (e.g. cyclohexanone[20]) diaziridines, which can easily be oxidized to the more stable diazirines.

3,3-Pentamethylendiaziridin durch Reaktion of Cyclohexanon mit HOSA

The reaction also provides substituted aziridines from simple aldehydes and ketones with high yield and diastereoselectivity.[21]

Synthesis of Diaziridinen with HOSA

1,2-Benzisoxazole is efficiently produced by nucleophilic attack of hydroxylamine-O-sulfonic acid to the carbonyl group of 2-hydroxybenzaldehyde followed by cyclization.[22]

Synthesis of 1,2-Benzisoxazol aus Salicylaldehyd und HOSA

1,2-Benzisoxazole is a structural element in the antipsychotic risperidone and paliperidone, as well as the anticonvulsant zonisamide.

In a one-pot reaction, N-aryl[3,4-d]pyrazolopyrimidines are obtained in good yields from simple 4,6-dichloropyrimidine-5-carboxaldehyde,[23]

N-Aryl-Pyrazolopyrimidine

which can be used as purine analogs for a wide range of diagnostic and therapeutic applications.[24]

Further reactions

The chemiluminescence of the system luminol/cobalt(II) chloride is dramatically enhanced by the addition of hydroxylamine-O-sulfonic acid.[25]

References

  1. ↑ 1.0 1.1 Matsuguma, Harold J.; Audrieth, Ludwig F.; Wehrmeister, Herbert L. (1957). "Hydroxylamine‐ O ‐Sulfonic Acid". Inorganic Syntheses. 5. 122–125. doi:10.1002/9780470132364.ch32. ISBN 9780470132364. 
  2. ↑ 2.0 2.1 2.2 Wiberg, Egon; Wiberg, Nils (2001). "Sulfur Compounds of Nitrogen". Inorganic Chemistry. Academic Press. pp. 675–677. ISBN 978-0-12-352651-9. https://books.google.com/books?id=Mtth5g59dEIC&pg=PA676. 
  3. ↑ 3.0 3.1 Wallace, Raymond G. (1980). "Hydroxylamine-O-sulfonic acid – a versatile synthetic reagent". Aldrichimica Acta 13 (1): 3–11. http://www.sigmaaldrich.com/ifb/acta/v13/acta-vol13-1980.html#3/zoomed. 
  4. ↑ Rademacher, P. (2014). "Product Class 7: Hydrazines and Hydrazinium Salts (40.7.1.1.9.2 – Using Hydroxylamine-O-sulfonic Acids". in Enders, Dieter; Schaumann, E.. Compounds with One Saturated Carbon–Heteroatom Bond: Amine N-Oxides, Haloamines, Hydroxylamines and Sulfur Analogues, and Hydrazines. Science of Synthesis: Houben-Weyl Methods of Molecular Transformations. 40b. Georg Thieme Verlag. p. 1171. ISBN 978-3-13-172181-5. https://books.google.com/books?id=MCGGAwAAQBAJ&pg=PA1171. 
  5. ↑ Wehrmeister, Herbert L. & Harold I. Yalowitz, "Process for the preparation of hydroxylamine-O-sulfonic acid", US patent 3281209, published 1966-10-25, issued 1966-10-25, assigned to Commercial Solvents Corporation
  6. ↑ Sommer, F.; Schulz, O. F.; Nassau, M. (1925). "Über die Sulfoperamidsäure" (in German). Z. Anorg. Allg. Chem. 147 (1): 142–155. doi:10.1002/zaac.19251470115. 
  7. ↑ Rathke, Michael W.; Millard, Alan A. (1978). "Boranes in functionalization of olefins to amines: 3-Pinanamine (Bicyclo[3.1.1heptan-3-amine, 2,6,6-trimethyl-)"]. Organic Syntheses 58: 32. doi:10.15227/orgsyn.058.0032. http://www.orgsyn.org/demo.aspx?prep=CV6P0943. ; Collective Volume, 6, pp. 943 
  8. ↑ Baenziger, Norman C.; Belt, Roger F.; Goebel, Carol V. (1967). "Crystal structure of hydroxylamine-O-sulfonic acid". Inorg. Chem. 6 (3): 511–514. doi:10.1021/ic50049a017. 
  9. ↑ Erdik, Ender (2001). "Hydroxylamine-O-Sulfonic Acid". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rh058. ISBN 978-0-471-93623-7. 
  10. ↑ R. Gösl; A. Meuwsen (1963). "1-Aminopyridinium iodide" (in German). Org. Synth. 43: 1. doi:10.15227/orgsyn.043.0001. 
  11. ↑ J. Streith (1991). "The Photochemistry of N-Iminopyridinium Ylides in Retrospect. From a Simple Concept to Some Applications" (in German). CHIMIA 45 (3): 65–76. 
  12. ↑ J. Streith (1977). "The photochemistry of aromatic-N-ylides. Rearrangement and fragmentation patterns" (in German). Pure Appl. Chem. 49 (3): 305–315. doi:10.1351/pac197749030305. 
  13. ↑ Campbell, C.D.; Rees, C.W. (1969). "Reactive intermediates. Part I. Synthesis and oxidation of 1- and 2-aminobenzotriazole". J. Chem. Soc. C 1969 (5): 742–747. doi:10.1039/J39690000742. 
  14. ↑ T.M. Klapötke; D.G. Piercey; J. Stierstorfer (2012). "Amination of energetic anions: high-performing energetic materials" (in German). Dalton Trans. 41 (31): 9451–9459. doi:10.1039/C2DT30684K. PMID 22751656. 
  15. ↑ R. Appel; W. Büchner; E. Guth (1958). "Zur Kenntnis des Imins, I. Über Phosphinimine und Sulfinimine" (in German). Justus Liebigs Ann. Chem. 618 (1): 53–58. doi:10.1002/jlac.19586180107. 
  16. ↑ S.L. Graham; T.H. Scholz (1986). "The reaction of sulfinic acid salts with hydroxylamine-O-sulfonic acid. A useful synthesis of primary sulfonamides" (in German). Synthesis 1986 (2): 1031–1032. doi:10.1055/s-1986-31862. 
  17. ↑ J. Streith; C. Fizet (1977). "Nucleophilic versus electrophilic properties of the nitrogen atom in O-sulfonyl-hydroxylamine derivatives" (in German). Tetrahedron Lett. 18 (37): 3297–3300. doi:10.1016/S0040-4039(01)83223-8. 
  18. ↑ C. Fizet; J. Streith (1974). "Hydroxylamine-O-sulfonic acid: A convenient reagent for the oxidative conversion of aldehydes into nitriles" (in German). Tetrahedron Lett. 15 (36): 3187–3188. doi:10.1016/S0040-4039(01)91857-X. 
  19. ↑ G.A. Olah; A.P. Fung (1985). "Hexahydro-2-(1H)-azocinone" (in German). Org. Synth. 63: 188. doi:10.15227/orgsyn.063.0188. 
  20. ↑ E. Schmitz; R. Ohme (1965). "3,3-Pentamethylenediaziridine" (in German). Org. Synth. 45: 83. doi:10.15227/orgsyn.045.0083. 
  21. ↑ A.W. Beebe; E.F. Dohmeier; G. Moura-Letts (2015). "Diastereoselective synthesis of substituted diaziridines from simple ketones and aldehydes" (in German). Chem. Commun. 51 (70): 13511–13514. doi:10.1039/C5CC04813C. PMID 26216745. 
  22. ↑ D.S. Kemp; R.B. Woodward (1965). "The N-ethylbenzisoxazolium cation—I : Preparation and reactions with nucleophilic species" (in German). Tetrahedron 21 (11): 3019–3035. doi:10.1016/S0040-4020(01)96921-2. 
  23. ↑ L.E. Evans; M.D. Cheeseman; K. Jones (2012). "N–N Bond-Forming Cyclization for the One-Pot Synthesis of N-Aryl[3,4-dpyrazolopyrimidines"] (in German). Org. Lett. 14 (13): 3546–3549. doi:10.1021/ol301561a. PMID 22734502. 
  24. ↑ C. Morrill; S. Babu; N.G. Almstead; Y.-C. Moon (2013). "Synthesis of 1,4-disubstituted pyrazolo[3,4-d]pyrimidines from 4,6-dichloropyrimidine-5-carboxaldehyde: insights into selectivity and reactivity" (in German). Synthesis 45 (13): 1791–1806. doi:10.1055/s-0033-1338862. 
  25. ↑ M. Saqib; W. Gao; J. Lai; L. Qi; S. Majeed; M.R.H.S. Gilani; G. Xu (2015). "Hydroxylamine-O-sulfonic acid as an efficient coreactant for luminol chemiluminescence for selective and sensitive detection" (in German). Chem. Commun. 51 (30): 6536–6539. doi:10.1039/C5CC01090J. PMID 25766485. 



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