Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703556Generated: October 30, 2026

Cyclohexene → HCID 85893940, compound

https://huagongshe.com/reaction/1703556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantNitrogen oxide (N2O4)HCID 25352—
ReactantHCID 70610342HCID 70610342—
SolventChloroformHCID 6212—
ProductHCID 85893940HCID 85893940—

Reaction Steps

To a solution of 2.2 g. (5.8 mmoles) of 2-iodo-3-phenyl-7-benzofuranacetic acid, 1 g. (5.8 mmoles) of cyclohexene and 175 ml. of chloroform is added 0.9 g. (10 mmoles) of dinitrogen tetroxide in 15 ml. of chloroform. The mixture is stirred for 20 hours, washed with water and made basic with sodium hydroxide. The chloroform layer is acidified with hydrochloric acid, washed with water twice and dried, then evaporated to provide 2-nitro-3-phenyl-7-benzofuranacetic acid, identical to the sample prepared in Example 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04124704
Source datasetuspto-grants-1978_11
ORD IDord-027c116dbe47483b8ba5195dbaee18cc
Source noteuspto-grants-1978_11