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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653112Generated: October 31, 2026

Cyclohexene → HCID 178526908, compound

https://huagongshe.com/reaction/653112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantNitrogen oxide (N2O4)HCID 25352—
ReactantHCID 178419493HCID 178419493—
SolventAcetic AcidHCID 176—
ProductHCID 178526908HCID 178526908—

Reaction Steps

To a stirred solution of 1.9 g. (0.005 mole) of 2-bromo-3-phenyl-5-tetrazolylmethylbenzofuran in 50 ml. of warm acetic acid and 1 ml. of cyclohexene is added 1 g. of dinitrogen tetraoxide. The mixture is heated on a steam bath for 30 minutes, then cooled to ice bath temperature. The product is separated by filtration, washed with acetic acid and diethyl ether and recrystallized from ethanol to provide yellow needles of 2-nitro-3-phenyl-5(1H-tetrazol-5-ylmethyl)benzofuran, m.p. 245°-247° C. having the structure

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675320
Source datasetuspto-grants-1987_06
ORD IDord-99f4da955f5f4e5e85cf2b9a823b7f13
Source noteuspto-grants-1987_06