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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833690Generated: October 31, 2026

Cyclohexane → HCID 20333854, compound

https://huagongshe.com/reaction/1833690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
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 cyclohexane 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 numberUS04066782
Source datasetuspto-grants-1978_01
ORD IDord-18f33c65853545ecaffca25f752e6073
Source noteuspto-grants-1978_01