Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181810Generated: November 1, 2026

Cyclohexene → HCID 10344102, compound

https://huagongshe.com/reaction/2181810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantBoron tribromideHCID 25134—
ReactantHCID 10479890HCID 10479890—
SolventDichloromethaneHCID 6344—
ProductHCID 10344102HCID 1034410276%

Reaction Steps

A stirred and cooled solution of 4-{[6-ethyl-2-(3-methoxyphenyl)phenanthridin-5(6H)-yl]sulfonyl}phenol (0.645 g, 1.36 mmol) and cyclohexene (1.1 mL, 10.9 mmol) in dichloromethane (5 mL) was treated drop-wise under nitrogen at −30° C. with boron tribromide (1.03 mL, 10.9 mmol). After the addition was completed, the reaction mixture was allowed to warm to room temperature and stirred for four hours. The reaction was cooled to −30° C. and quenched with methanol (1 mL). The solvent was removed in vacuo, and the residue was purified by flash column chromatography on silica gel, eluting with a mixture of ethyl acetate-hexane (1:3); to yield the title compound (0.473 g, 1.03 mmol, 76%), which was characterized by LCMS (ES+, FA, CV=20 or 5), m.p. 105° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894061B2
Source datasetuspto-grants-2005_05
ORD IDord-9035e0e2444b4fb8b52790320eac3368
Source noteuspto-grants-2005_05