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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583006Generated: October 25, 2026

Sodium Acetate → N-(methoxycarbonyl)-4-keto-D-proline methyl ester

https://huagongshe.com/reaction/583006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactantracemic N-(methoxycarbonyl)-4-keto-D,L-proline methyl esterHCID 9837087—
ProductN-(methoxycarbonyl)-4-keto-D-proline methyl esterHCID 11275680—

Reaction Conditions

Temperature25 °C

Reaction Steps

A 200 mL aqueous solution containing 0.200M sodium acetate (pH 5.0), 1.3325 g of Candida antartica lipase fraction B, and 4.02 g of racemic N-(methoxycarbonyl)-4-keto-D,L-proline methyl ester (100 mM) was stirred at 25° C. After 24 h, an 96% enantiomeric excess of N-(methoxycarbonyl)-4-keto-D-proline methyl ester was obtained at 50% conversion of the racemic mixture. The reaction mixture was filtered using a 10,000 MWCO membrane filter (Amicon) to remove the enzyme catalyst, and the filtrate extracted with three 200 mL portions of dichloromethane. The combined organic extracts were dried over magnesium sulfate, filtered, and the dichloromethane removed from the filtrate by rotary evaporation at reduced pressure. Residual dichloromethane was removed from the resulting colorless oil at high vacuum (50 millitorr) to produce N-(methoxycarbonyl)-4-keto-D-proline methyl ester as a white solid (1.99 g, 99% isolated yield, 99% purity (by GC), 97% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05928933
Source datasetuspto-grants-1999_07
ORD IDord-8f4a9ba4283b426eb41f634417707f3f
Source noteuspto-grants-1999_07