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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658624Generated: October 31, 2026

Hydrochloric Acid → 1-(3-(Trifluoromethylthio)phenyl)propan-2-one

https://huagongshe.com/reaction/1658624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-(2-Nitroprop-1-en-1-yl)-3-[(trifluoromethyl)sulfanyl]benzeneHCID 53877630—
CatalystIronHCID 23925—
Product1-(3-(Trifluoromethylthio)phenyl)propan-2-oneHCID 2132526960.5%

Reaction Steps

13.2 g. (50 mmols) of 1-(3'-trifluoromethylthiophenyl)-2-nitro-propene, 19.6 g. (0.35 g. atom) of iron powder and 0.25 g. of ferric chloride are introduced into a 250 ml. three-necked flask equipped with a mechanical stirrer, a condenser and a dropping funnel, and this mixture is heated on an oil bath at 80°-90°C. 13.5 ml. of concentrated hydrochloric acid are added dropwise, via the dropping funnel, with stirring, over the course of 7 hours, while the temperature is kept at 90°C. The reaction mixture is allowed to cool and rendered alkaline with sodium hydroxide solution. The ketone is then steam distilled. The distillate is extracted twice in succession with 100 ml. of diethyl ether each time. The two ether extracts are combined, dried over sodium sulphate and filtered. The solvent is evaporated from the filtrate in vacuo on a water bath, and the residue is rectified. 7.1 g. (60.5% yield) of 1-(3'-trifluoromethylthiophenyl)-2-propanone are thus obtained as a colourless oil, b.p. 138°-146°C./25-30 mm. Hg., nD23 ° = 1.489.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03965190
Source datasetuspto-grants-1976_06
ORD IDord-6c62b65a98934f668de8197d2e9dc4a6
Source noteuspto-grants-1976_06