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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906948Generated: November 2, 2026

Ethyl Acetate → HCID 59557026, compound

https://huagongshe.com/reaction/906948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCerium(III) chlorideHCID 24636—
Reactantbenzyl (2S)-2-methyl-3-oxopyrrolidine-1-carboxylateHCID 59556933—
ReactantHCID 178467822HCID 178467822—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59557026HCID 5955702684%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A suspension (300 mL) of cerium chloride (47 g) in THF was cooled to −78° C., and 3 mol/L methylmagnesium bromide-diethyl ether solution (56 mL) was added dropwise while adjusting the temperature of the solution to not higher than −70° C. After the completion of the dropwise addition, the mixture was stirred at −78° C. for 30 min, and a solution (60 mL) of benzyl (2S)-2-methyl-3-oxopyrrolidine-1-carboxylate (18 g) in THF was added dropwise while adjusting the temperature of the solution to not higher than −70° C. The reaction mixture was warmed to 0° C. over 2 hr, ethyl acetate (1 L) was added, and the insoluble material was filtered off. Water was added to the filtrate and then the mixture was partitioned. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1→1/1) to give the title compound as a colorless oil (yield: 16.2 g, yield: 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013008B2
Source datasetuspto-grants-2011_09
ORD IDord-5019fcd52eeb4ddc8df167a380e9185c
Source noteuspto-grants-2011_09