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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967263Generated: October 30, 2026

Ethyl Acetate → HCID 59557026, compound

https://huagongshe.com/reaction/1967263

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 of cerium chloride (47 g) in THF (300 mL) was cooled to −78° C., methylmagnesium bromide-diethyl ether solution (56 mL, 3 mol/L) was added dropwise while adjusting the solution temperature to −70° C. or below. After the completion of the dropwise addition, the mixture was stirred at −78° C. for 30 min, a solution of benzyl (2S)-2-methyl-3-oxopyrrolidine-1-carboxylate (18 g) in THF (60 mL) was added dropwise while adjusting the solution temperature to −70° C. or below. The reaction mixture was warmed to 0° C. over 2 hr, ethyl acetate (1 L) was added, and insoluble materials were filtered off. The filtrate was partitioned with water, and 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, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420694B2
Source datasetuspto-grants-2013_04
ORD IDord-24a122ac8c804273a14aeb107b02d67e
Source noteuspto-grants-2013_04