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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859215Generated: November 2, 2026

Potassium Carbonate → HCID 68614531, compound

https://huagongshe.com/reaction/859215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluorobenzyl bromideHCID 68021—
ReactantMethyl 1-(4-hydroxyphenyl)-5-oxopyrrolidine-3-carboxylateHCID 2883518—
SolventMethyl Ethyl KetoneHCID 6569—
SolventEthyl AcetateHCID 8857—
ProductHCID 68614531HCID 6861453198.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 5.0 g (21.3 mmol) of (RS)-1-(4-hydroxy-phenyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester [Example 2 b)] in 200 ml of 2-butanone is treated with 3.55 ml (27.6 mmol) of 4-fluorobenzyl-bromide and 5.88 g (42.5 mmol) of potassium carbonate and the mixture is stirred at 90° C. for 3 hours. For the working-up, the reaction mixture is diluted with ethyl acetate and extracted with water. The organic phase is separated, dried over sodium sulfate and evaporated under reduced pressure. For purification, the material obtained is chromatographed on silica gel using a 98:2-mixture dichloromethane and methanol as the eluent. There are obtained 7.18 g (98% of theory) of (RS)-1-[4-(4-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methyl ester as a white solid. MS: m/e=344 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151111B2
Source datasetuspto-grants-2006_12
ORD IDord-c6b8a5f46e694e2495783eaced23c9bb
Source noteuspto-grants-2006_12