Chemistry:Prolinol
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| IUPAC name
(R/S) 2-pyrrolidinemethanol
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3D model (JSmol)
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| Properties | |||
| C5H11NO | |||
| Molar mass | 101.149 g·mol−1 | ||
| Appearance | Liquid | ||
| Density | 1.036 g/mL (liquid) | ||
| Boiling point | 74–76 °C (165–169 °F; 347–349 K) at 2 mmHg | ||
| Hazards | |||
| Main hazards | Irritant | ||
| GHS pictograms | 
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| GHS Signal word | Warning | ||
| H315, H319, H335 | |||
| P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501 | |||
| Flash point | 86 °C (187 °F; 359 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
 verify (what is   ?)
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Prolinol is a chiral amino-alcohol that is used as a chiral building block in organic synthesis. It exists as two enantiomers: the D and L forms.
Preparation
Prolinol is obtained by reduction of the amino acid proline using lithium aluminium hydride.[2][3] Because proline is cheaply available in high optical purity, enantiomerically pure prolinol is also widely available.
Use
Prolinol is used in broad variety of chemical reactions as chiral ligand, chiral catalyst or chiral auxiliary reagent in the Hajos–Parrish–Eder–Sauer–Wiechert reaction, the Baylis–Hillman reaction, Noyori type reactions and the Michael reaction. [4][5]
See also
References
- ↑ "D-Prolinol" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/2724541#section=Safety-and-Hazards.
- ↑ Dickman, D. A.; Meyers, A. I.; Smith, G. A.; Gawley, R. E.. "Reduction of α-Amino Acids: L-Valinol". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=CV7P0530.; Collective Volume, 7, pp. 530
- ↑ Enders, D.; Fey, P.; Kipphardt, H.. "(S)-(–)-1-Amino-2-Methoxymethylpyrrolidine (SAMP) and (R)-(+)-1-Amino-2-Methoxymethylpyrrolidine (RAMP), Versatile Chiral Auxiliaries". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=CV8P0026.; Collective Volume, 8, pp. 26
- ↑ Benjamin List (2002). "Proline-catalyzed asymmetric reactions". Tetrahedron 58 (28): 5573–5590. doi:10.1016/S0040-4020(02)00516-1.
- ↑ Shinichi Itsuno; Koichi Ito; Akira Hirao; Seiichi Nakahama (1984). "Asymmetric synthesis using chirally modified borohydrides. Part 2. Enantioselective reduction of ketones with polymeric (S)-prolinol–borane reagent". J. Chem. Soc., Perkin Trans. 1 (12): 2887–2895. doi:10.1039/P19840002887.
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