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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703478Generated: November 1, 2026

Cyclohexene → HCID 20333854, compound

https://huagongshe.com/reaction/1703478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantNitrogen oxide (N2O4)HCID 25352—
ReactantHCID 20333853HCID 20333853—
SolventChloroformHCID 6212—
ProductHCID 20333854HCID 20333854—

Reaction Steps

A solution of 3-(2-bromo-5-chloro-3-benzofuranyl)-phenylacetic acid in chloroform with 1.5 equivalents of cyclohexene is treated with 1.5 equivalents of dinitrogen tetroxide and stirred for about 20 hours at room temperature. The mixture is washed with water, extracted with saturated sodium bicarbonate solution, then the aqueous extracts are acidified. The mixture is extracted with dichloromethane, which is dried and concentrated. The residue is recrystallized from a mixture of benzene and hexane to provide 3-(5-chloro-2-nitro-3-benzofuranyl)phenylacetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04124605
Source datasetuspto-grants-1978_11
ORD IDord-6cdbee8f698f47e9aae7b7889996c683
Source noteuspto-grants-1978_11