2-(S)-Hydroxy-3-methylbutyric acid methyl ester

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2-(S)-Hydroxy-3-methylbutyric acid methyl ester Basic information
Uses
Product Name:2-(S)-Hydroxy-3-methylbutyric acid methyl ester
Synonyms:2-(S)-Hydroxy-3-methylbutyric acid methyl ester;(S)-Methyl 2-hydroxy-3-methylbutanoate;methyl (S)-2-hydroxy-3-methylbutanoate;Butanoic acid, 2-hydroxy-3-methyl-, methyl ester, (2S)-;methyl (2s)-2-hydroxy-3-methylbutanoate;(S)-Methyl 2-hydroxy-3-methylbutanoate - [M92121]
CAS:24347-63-5
MF:C6H12O3
MW:132.16
EINECS:
Product Categories:
Mol File:24347-63-5.mol
2-(S)-Hydroxy-3-methylbutyric acid methyl ester Structure
2-(S)-Hydroxy-3-methylbutyric acid methyl ester Chemical Properties
Boiling point 61-62 °C(Press: 15 Torr)
density 1.021±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka12.94±0.20(Predicted)
form liquid
color Colourless
LogP0.160 (est)
Safety Information
HS Code 2918199890
MSDS Information
2-(S)-Hydroxy-3-methylbutyric acid methyl ester Usage And Synthesis
Uses(S)-Methyl 2-hydroxy-3-methylbutanoate is a useful research chemical.
Synthesis
Methanol

67-56-1

(S)-(+)-2-HYDROXY-3-METHYLBUTYRIC ACID

17407-55-5

2-(S)-Hydroxy-3-methylbutyric acid methyl ester

24347-63-5

Methanol (14.5 mL, 360 mmol) and p-toluenesulfonic acid monohydrate (0.68 g, 3.6 mmol) were added to a solution of (S)-(+)-2-hydroxy-3-methylbutyric acid (14.20 g, 120 mmol) in carbon tetrachloride (40 mL). The reaction mixture was refluxed under anhydrous conditions for 10 hours. Upon completion of the reaction, the mixture was cooled to room temperature, washed sequentially with water (15 mL) and saturated aqueous sodium bicarbonate solution (10 mL), dried over magnesium sulfate, and concentrated under reduced pressure. Purification of the residue by distillation afforded methyl (S)-2-hydroxy-3-methylbutanoate (13.03 g, 82% yield) as a colorless oil; boiling point 62-63 °C/15 Torr; specific optical rotation [α]D = +23.7 (c 1.00, CHCl3), literature value [α]D = +24.3 (c 1.00, CHCl3); 1H NMR ( CDCl3) δ 0.82 (d, J = 6.9 Hz, 3H, 3-Me), 0.98 (d, J = 6.9 Hz, 3H, 3-Me), 2.03 (m, 1H, 3-H), 2.83 (d, J = 6.2 Hz, 1H, OH), 3.75 (s, 3H, CO2Me), 4.01 (dd, J = 6.2, 3.6 Hz 1H, 2-H); 13C NMR (CDCl3) δ 15.9, 18.6, 32.1, 52.2, 75.0, 175.3; IR (thin film) νmax: 3483, 1735 cm-1.

References[1] Journal of the American Chemical Society, 1990, vol. 112, # 21, p. 7659 - 7672
[2] Tetrahedron Letters, 1989, vol. 30, # 29, p. 3757 - 3760
[3] Journal of Chemical Research, Miniprint, 1998, # 1, p. 126 - 142
[4] Heterocycles, 1999, vol. 51, # 6, p. 1321 - 1343
[5] Organic and Biomolecular Chemistry, 2005, vol. 3, # 20, p. 3749 - 3756
2-(S)-Hydroxy-3-methylbutyric acid methyl ester Preparation Products And Raw materials
Raw materialsMethanol-->(S)-(+)-2-HYDROXY-3-METHYLBUTYRIC ACID-->2-ACETOXY-3-METHYL-BUTYRIC ACID-->Carbon tetrachloride-->p-Toluenesulfonic acid monohydrate
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