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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210635Generated: November 2, 2026

Hydrochloric Acid → 1-(3,4-dimethoxyphenyl)-4,4,4-trifluorobutane-1,3-dione

https://huagongshe.com/reaction/2210635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl trifluoroacetateHCID 9794—
Reactant3,4-Dimethoxyphenyl methyl ketoneHCID 14328—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(3,4-dimethoxyphenyl)-4,4,4-trifluorobutane-1,3-dioneHCID 691720396%

Reaction Conditions

Temperature50 °C

Reaction Steps

216 g (4 mol) of anhydrous sodium methylate and 3.5 l of toluene are introduced into a 10 liter round-bottomed flask and, under vigorous stirring, 705 g (5 mol) of ethyl trifluoroacetate are then run in; the temperature rises slowly to 30° C. After cooling in an ice bath, a solution of 720 g (4 mol) of 3,4-dimethoxyacetophenone in 0.5 l of toluene is added dropwise to the reaction mixture; a white precipitate slowly forms. The mixture is next left stirred overnight and then heated to 50° C. for three hours. After cooling, 2 1 of water and 330 ml of concentrated hydrochloric acid are added, the organic phase is separated off after settling has taken place, dried over magnesium sulphate, filtered and evaporated to obtain 1060 g (96%) of a yellow solid melting at 87°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05459262
Source datasetuspto-grants-1995_10
ORD IDord-ced4b3146bce44aeb88c5de9966e7e24
Source noteuspto-grants-1995_10