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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164303Generated: November 4, 2026

Diethyl Ether → HCID 20511711, compound

https://huagongshe.com/reaction/1164303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
Reactant2-PyrrolidoneHCID 12025—
Reactant4-BenzyloxybenzoylchlorideHCID 3766410—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 20511711HCID 20511711—

Reaction Steps

15.9 g. of p-benzyloxybenzoyl chloride, 500 ml. of absolute diethyl ether and 6.3 ml. of 2-pyrrolidinone are treated with 13.4 ml. of triethylamine at 0° C. to 10° C. while stirring. The mixture is stirred at reflux for 9 hours, then cooled down and treated at 0° C. with cold water and ethyl acetate. The organic phase is washed with water, dried over sodium sulfate and evaporated. The residue is triturated with diethyl ether and the insoluble constituents are chromatographed over silica gel (particle size 0.2-0.5 mm). The constituents elutable with methylene chloride are triturated with diethyl ether. The insoluble constituents are filtered off and there is obtained 1-(p-benzyloxybenzoyl)-2-pyrrolidinone, having a melting point of 115°-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04369139
Source datasetuspto-grants-1983_01
ORD IDord-d6fbf48280fc45ce889bd6505b20a32a
Source noteuspto-grants-1983_01