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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250835Generated: October 27, 2026

Hydrochloric Acid → methyl(E)-3-(3-fluoro-4-trifluoromethanesulfonyloxyphenyl)acrylate

https://huagongshe.com/reaction/250835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantDiisopropylethylamineHCID 81531—
Reactantmethyl(E)-3-(3-fluoro-4-hydroxyphenyl)acrylateHCID 67273036—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productmethyl(E)-3-(3-fluoro-4-trifluoromethanesulfonyloxyphenyl)acrylateHCID 86614973102%

Reaction Steps

1.40 mL (8.3 mmol, 1.1 eq) of triflic anhydride are added to a solution of 1.47 g (7.5 mmol, 1 eq) of methyl (E)-3-(3-fluoro-4-hydroxyphenyl)acrylate and 1.57 mL (9.0 mmol, 1.2 eq) of diisopropylethylamine in 10 mL of dichloromethane. The reaction mixture is stirred at room temperature overnight. The reaction medium is hydrolyzed in water, acidified with 1N hydrochloric acid solution and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over sodium sulfate. The solvent is evaporated off and 2.51 g of methyl (E)-3-(3-fluoro-4-trifluoromethanesulfonyloxyphenyl)acrylate are obtained in the form of a brown oil. Yield=100%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863332B2
Source datasetuspto-grants-2011_01
ORD IDord-e025e15aeaf14fde97eea05cd14db590
Source noteuspto-grants-2011_01