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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858270Generated: October 29, 2026

p-Toluenesulfonic acid → 7-Bromo-4,4-dimethylthiochroman

https://huagongshe.com/reaction/858270

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 18768217HCID 18768217—
SolventTolueneHCID 1140—
Product7-Bromo-4,4-dimethylthiochromanHCID 2239309990.5%

Reaction Steps

25.00 g (97.0 mmol) of 1-bromo-3-(3-methylbut-2-enylsulphonyl)benzene, 200 ml of toluene and 27.75 g (146.0 mmol) of para-toluenesulphonic acid are introduced into a three-necked flask. The reaction medium is refluxed for four hours and 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 has taken place, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with heptane. 22.57 g (90%) of the expected compound are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148245B2
Source datasetuspto-grants-2006_12
ORD IDord-ef75afe850a246058183ba50cc54a66d
Source noteuspto-grants-2006_12