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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897071Generated: October 25, 2026

p-Toluenesulfonic acid → HCID 22252737, compound

https://huagongshe.com/reaction/897071

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, 180 ml of toluene and 23.20 g (122.0 mmol) of para-toluenesulphonic acid are introduced into a three-necked flask. The reaction medium is refluxed for four hours and is then evaporated to dryness. The residue is taken up in aqueous sodium hydrogen carbonate solution and extracted with ethyl acetate, and the organic phase is separated out after settling, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a column of silica and eluted with heptane. 20 g (76%) of the expected compound are collected in the form of an orange-coloured oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921777B2
Source datasetuspto-grants-2005_07
ORD IDord-89f26375daa94ebbba35d32459cff721
Source noteuspto-grants-2005_07