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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071930Generated: November 2, 2026

Trifluoromethanesulfonic anhydride → HCID 22390454, compound

https://huagongshe.com/reaction/1071930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 22390446HCID 22390446—
SolventPyridineHCID 1049—
SolventTolueneHCID 1140—
ProductHCID 22390454HCID 22390454—

Reaction Steps

8.2 ml of triflic anhydride are added at 5° C. to 9.7 g of 2-chloro-4-(4,4-dimethylcyclohexyl)phenol (compound IX.1) in 60 ml of pyridine, the reaction mixture is left to stand for 30 minutes at 0° C., and then the reaction mixture is stirred at room temperature for 12 hours. The reaction mixture is hydrolysed and then extracted with dichloromethane. The organic phase is dried over magnesium sulphate and the solvents are evaporated off under reduced pressure. The residue obtained is taken up in toluene, and then the solvents are evaporated off under reduced pressure. The residue obtained is purified by chromatography on a column of silica gel, eluting with a cyclohexane/ethyl acetate mixture which varies from 100/0 to 99/1 (v/v). 15 g of the compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908914B1
Source datasetuspto-grants-2005_06
ORD IDord-c849e5f47c714cc0bc66f7d97c477071
Source noteuspto-grants-2005_06