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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26243Generated: October 29, 2026

Hydrochloric Acid → 1-[3-(Trifluoromethoxy)phenyl]propan-2-one

https://huagongshe.com/reaction/26243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant1-(3'-Trifluoromethoxyphenyl)-2-nitro-propeneHCID 53911105—
CatalystIronHCID 23925—
Product1-[3-(Trifluoromethoxy)phenyl]propan-2-oneHCID 2132527155%

Reaction Conditions

Temperature80 °C

Reaction Steps

29 g (117 mmols) of 1-(3'-trifluoromethoxy-phenyl)-2-nitro-propene, 46 g (0.82 g atom) of iron powder, 0.6 g of ferric chloride and 120 ml of water are introduced into a 500 ml three-necked flask equipped with a mechanical stirrer, a condenser and a dropping funnel, and this mixture is heated at 80° C. 29 ml of concentrated hydrochloric acid are added dropwise, via the dropping funnel, with stirring, over the course of 5 hours, while the temperature is kept at 80° C. The reaction mixture is allowed to cool overnight. 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. 14,15 g (55% yield) of 1-(3'-trifluoromethoxy-phenyl)-2-propanone are thus obtained as a liquid, b.p. 112°- 118° C./18 mm.Hg, nD21°5 =1.448.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04148923
Source datasetuspto-grants-1979_04
ORD IDord-8c9b93c0c5ea4767bdd610ba686675cd
Source noteuspto-grants-1979_04