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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266445Generated: October 31, 2026

Chloromethyl phenyl sulphide → HCID 70044820, compound

https://huagongshe.com/reaction/266445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl phenyl sulphideHCID 81623—
Reactant133743-22-3HCID 14257493—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 70044820HCID 7004482084%

Reaction Steps

A mixture of 3.27 g (0.012 mol) of 4-bromosaccharin [Japanese Pat. Publcn. 58/79,034, published May 12, 1983; C. A. 100, 7773w (1984)], 1.63 g (0.015 mol) of potassium t-butoxide, 0.39 g (0.0012 mol) of tetrabutylammonium bromide and 3.0 ml (0.022 mol) of chloromethyl phenyl sulfide in 100 ml of toluene was heated under reflux under a nitrogen atmosphere for eight hours and then at ambient temperature for about sixteen hours. The reaction mixture was then cooled, diluted with ethyl acetate and the organic layer washed with bicarbonate, water and brine and then dried over magnesium sulfate and taken to dryness in vacuo. The residual solid was recrystallized from toluene-hexane to give 3.86 g (84%) of 4-bromo-2-phenylthiomethylsaccharin, mp 174.5°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650422
Source datasetuspto-grants-1997_07
ORD IDord-03e9ebc55f2f4b84976700a702e8865d
Source noteuspto-grants-1997_07