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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471354Generated: October 26, 2026

Diethyl 2-t-butyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate → (R)-1-benzyl hydrogen 3-t-butyloxycarbonylamino-3-ethoxycarbonylsuccinate

https://huagongshe.com/reaction/471354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl 2-t-butyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonateHCID 66725227—
SolventPhosphateHCID 1061—
SolventAcetonitrileHCID 6342—
Product(R)-1-benzyl hydrogen 3-t-butyloxycarbonylamino-3-ethoxycarbonylsuccinateHCID 66725181—

Reaction Conditions

Temperature30 °C

Reaction Steps

1.0 g of pig liver esterase produced by Sigma [PLE (27 kU/g), lyophilized product, product number: E3019] was dissolved in a 0.1 mol/L phosphate buffer adjusted to pH 7.5 (90 mL), and the solution was added with a solution of diethyl 2-t-butyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate (1.0 g) dissolved in acetonitrile (10 mL). The mixture was stirred at 30° C. for 4 hours to produce the title compound. Optical purity measured by HPLC was 78.1% ee. After completion of the reaction, the reaction mixture was filtered by using a filtration aid (KC Floc 100) to remove the insoluble matter. The filtrate was cooled, and adjusted to pH 2 by adding 6 mol/L hydrochloric acid, then the objective substance was extracted with ethyl acetate, and the extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain the title compound (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633001B2
Source datasetuspto-grants-2014_01
ORD IDord-52ab5c6af580476a91e64bca975e4fce
Source noteuspto-grants-2014_01