Chemistry:Trimethyl orthoformate
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| Preferred IUPAC name
Trimethoxymethane | |
| Other names
2-Methoxyacetaldehyde dimethyl acetal; Methoxymethylal; Methyl orthoformate
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| Identifiers | |
3D model (JSmol)
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| Properties | |
| C4H10O3 | |
| Molar mass | 106.121 g·mol−1 |
| Appearance | Colorless liquid |
| Odor | pungent |
| Density | 0.9676 g/cm3 |
| Melting point | −53 °C (−63 °F; 220 K) |
| Boiling point | 100.6 °C (213.1 °F; 373.8 K) |
| Solubility | soluble in ethanol, diethyl ether |
| Vapor pressure | 1 kPa at 7 °C[2] |
Refractive index (nD)
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1.3773 |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H225, H315, H319, H335 | |
| P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+352, P303+361+353, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P370+378, P403+233, P403+235, P405, P501 | |
| Flash point | 13 °C (55 °F; 286 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Trimethyl orthoformate (TMOF) is the organic compound with the formula HC(OCH3)3. A colorless liquid, it is the simplest orthoester. It is a reagent used in organic synthesis for the formation of methyl ethers.[3] The product of reaction of an aldehyde with trimethyl orthoformate is an acetal. In general cases, these acetals can be deprotected back to the aldehyde by using hydrochloric acid.
Synthesis
Trimethyl orthoformate is prepared on an industrial scale by the methanolysis of hydrogen cyanide:[4]
- HCN + 3 HOCH3 → HC(OCH3)3 + NH3
Trimethyl orthoformate can also be prepared from the reaction between chloroform and sodium methoxide, an example of the Williamson ether synthesis.
Use
Trimethyl orthoformate is a useful building block for creating methoxymethylene groups and heterocyclic ring systems. It introduces a formyl group to a nucleophilic substrate, e.g. RNH2 to form R-NH-CHO, which can undergo further reactions. It is used in the production of the fungicides, azoxystrobin, and picoxystrobin, as well as for some members of the floxacin family of antibacterial drugs.
A number of pharmaceutical intermediates are also made from trimethyl orthoformate.[4]
Trimethyl orthoformate is also an effective reagent for converting compatible carboxylic acids to their corresponding methyl esters.[5] Alternatively, acid-catalyzed esterifications with methanol can be driven closer to completion by employing trimethyl orthoformate to convert water byproduct to methanol and methyl formate.
See also
References
- ↑ Trimethyl orthoformate at Sigma-Aldrich
- ↑ Alfa Aesar SDS
- ↑ Liu, Hui; Tomooka, Craig S.; Xu, Simon L.; Yerxa, Benjamin R.; Sullivan, Robert W.; Xiong, Yifeng; Moore, Harold W. (1999). "Dimethyl Squarate and ITS Conversion to 3-Ethenyl-4-Methoxycyclobutene-1,2-Dione and 2-Butyl-6-Ethenyl-5-Methoxy-1,4-Benzoquinone". Organic Syntheses 76: 189. doi:10.15227/orgsyn.076.0189.
- ↑ 4.0 4.1 Ashford's Dictionary of Industrial Chemicals, Third edition, 2011, ISBN:978-0-9522674-3-0, page 9388
- ↑ Paine, John B. (1 July 2008). "Esters of Pyromellitic Acid. Part I. Esters of Achiral Alcohols: Regioselective Synthesis of Partial and Mixed Pyromellitate Esters, Mechanism of Transesterification in the Quantitative Esterification of the Pyromellitate System Using Orthoformate Esters, and a Facile Synthesis of the Ortho Pyromellitate Diester Substitution Pattern". The Journal of Organic Chemistry 73 (13): 4929–4938. doi:10.1021/jo800543w.
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