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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664221Generated: October 31, 2026

Allyl bromide → HCID 67439909, compound

https://huagongshe.com/reaction/1664221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67438703HCID 67438703—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67439909HCID 67439909—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 3.69 g (8.1 mmol) 3-benzyloxycarbonylamino-5-(2-oxo-pyrrolidin-1-yl)-benzoic acid methyl ester, 1.37 ml (16.2 mmol) allyl bromide, 2.24 g (16.2 mmol) potassium carbonate in 8 ml DMF is stirred at 50° C. for 4 h. The mixture is diluted with water and extracted with EtOAc. The organic phase is washed with water and dried over sodium sulfate. The product is purified by chromatography on silica gel (EtOAc/hexanes 1:4, 1:2, 1:1, 2:1). The title compound is isolated as a yellow resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039455B2
Source datasetuspto-grants-2011_10
ORD IDord-a14a8cfbe89144aea7f5b384b93304e7
Source noteuspto-grants-2011_10