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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388539Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 12815947, compound

https://huagongshe.com/reaction/1388539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 12815944HCID 12815944—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
ProductHCID 12815947HCID 1281594777.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 55.7 g of crude 2-chloromethyl-4-(trifluoromethylthio)chlorobenzene, 23 g of potassium acetate, 150 ml of dimethyl sulfoxide and 10 g of triethylbenzylammonium chloride is stirred for 5 hours at 60° C. It is decomposed by pouring into water, extracted with benzene and the benzene evaporated. The oily residue is dissolved in 200 ml of ethanol, 100 ml of water and 20 ml of hydrochloric acid are added and the mixture is stirred and refluxed for 7 hours. Ethanol is distilled off, the residue mixed with water and extracted with benzene. The oil obtained by evaporation of the dried extract, is distilled in vacuo. There are obtained 40.2 g crude 2-chloro-5-(trifluoromethylthio)benzyl alcohol boiling at 140°-150° C./2 kPa. According to the 1H-NMR spectrum the product contains approximately 80% of the named compound and the remainder is the position isomer. In this state the substance is suitable for further processing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431808
Source datasetuspto-grants-1984_02
ORD IDord-850dc277fe464c80af6cdc1cd06e7244
Source noteuspto-grants-1984_02