Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22992Generated: October 26, 2026

p-Toluenesulfonic acid → HCID 22252737, compound

https://huagongshe.com/reaction/22992

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Bromo-1-(3-methylbut-2-enylthio)benzeneHCID 10634875—
SolventTolueneHCID 1140—
ProductHCID 22252737HCID 22252737—

Reaction Steps

26.00 g (102.0 mmol) of 2-bromo-1-(3-methylbut-2-enylthio)benzene, 130 ml of toluene and 23.20 g (122.0 mmol) of para-toluenesulphonic acid are introduced into a three-necked flask. The reaction mixture is heated at reflux for four hours and is evaporated to dryness. The residue is taken up in an aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate and the organic phase is separated by settling, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column eluted with heptane. 20.00 g (76%) of the expected compound are collected in the form of an orangey oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849658B2
Source datasetuspto-grants-2005_02
ORD IDord-e085397cc5d5450497a7d3d8009c06a4
Source noteuspto-grants-2005_02