Sodium Hydroxide → HCID 11240950, compound

500 ml of toluene containing 100 g of racemic methyl 2,3-epoxy-3-cyclohexylpropionate, was added to 500 ml of a 1M tris-HCl buffer solution (pH 8.0) containing lipase (derived from hog pancreas, manufactured by Wako Pure Chemical Industries, Ltd.) in a concentration of 5 g/l, and asymmetric hydrolysis reaction was carried out at 30° C. for 48 hours at a stirring speed of 600 rpm. After the reaction, a 1N sodium hydroxide aqueous solution was added to the reaction solution to adjust the pH of the aqueous phase to 10, whereupon the aqueous phase was separated. The aqueous phase was then adjusted to pH 2 with a 1N hydrochloric acid solution, and then, extracted twice with 300 ml of t-butyl methyl ether. The organic layer was concentrated under reduced pressure to obtain 42.5 g of (2R,3S)-2,3-epoxy-3-cyclohexylpropionic acid as crude crystals. The crude crystals were dissolved in 200 ml of a solution of toluene/n-heptane=1/2 (v/v) and heated and dissolved for 20 minutes with stirring at 60° C. The solution was gradually cooled from 60° C. to 20° C. and then cooled with ice for 30 minutes, whereupon precipitated crystals were collected by filtration to obtain 40.2 g of crystals of (2S,3R)-2,3-epoxy-3-cyclohexylpropionic acid (98.6% ee [α]D2=−20.8 (c 1.04, CHCl3)).

1. additioncontaining lipase (derived from hog pancreas, manufactured by Wako Pure Chemical Industries, Ltd.)
2. customin a concentration of 5 g/l, and asymmetric hydrolysis reaction
3. customAfter the reaction
4. customwhereupon the aqueous phase was separated
5. extractionextracted twice with 300 ml of t-butyl methyl ether
6. concentrationThe organic layer was concentrated under reduced pressure

ORD record

ord-b70b0b851b9d4007979de6dc680b5c5f

Source dataset

uspto-grants-2007_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07169944B2