Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703551Generated: November 2, 2026

Cyclohexane → HCID 85893940, compound

https://huagongshe.com/reaction/1703551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
ReactantNitrogen oxide (N2O4)HCID 25352—
ReactantHCID 70609418HCID 70609418—
SolventChloroformHCID 6212—
ProductHCID 85893940HCID 85893940—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-bromo-3-phenyl-4-benzofuranacetic acid (12.1 g., 0.0365 mole) and cyclohexane (3.3 g., 0.04 mole) in 100 ml. of chloroform is treated with 5 g. of dinitrogen tetroxide in 20 ml. of chloroform dropwise. The mixture is stirred for 16 hours at about 25° C. then at 50°-55° C. for about 20 minutes. The mixture is washed with water, and the organic layer is treated with an aqueous base. The aqueous layer is acidified, then extracted with dichloromethane. The organic layer is washed thrice with water, dried and evaporated. Two recrystallizations from benzene give light yellow solid 2-nitro-3-phenyl-4-benzofuranacetic acid, m.p. 187.5°-189.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04124704
Source datasetuspto-grants-1978_11
ORD IDord-e7e9fab63a1942be89035f473b0d32f3
Source noteuspto-grants-1978_11