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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637612Generated: October 31, 2026

Hydrochloric Acid → 2-[3-Fluoro-4-(2,2,2-trichloroethyl)phenyl]propionic acid

https://huagongshe.com/reaction/637612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitriteHCID 946—
ReactantVinylidene chlorideHCID 6366—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(4-Amino-3-fluorophenyl)propanoic acidHCID 13065231—
SolventAcetoneHCID 180—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product2-[3-Fluoro-4-(2,2,2-trichloroethyl)phenyl]propionic acidHCID 13564324—

Reaction Steps

In 10 ml of a 17% aqueous hydrochloric acid solution was dissolved 2.5 g of 2-(4-amino-3-fluorophenyl)propionic acid. To the solution was added dropwise 5 ml of an aqueous solution of 1.04 g of sodiun nitrite at -15° C.--10° C. with stirring, and the reaction was carried out for an hour. To the mixture were added 25 ml of acetone and 3 g of 1,1-dichloroethylene at -10° C.--5° C., followed by 2.5 g of sodium hydrogen carbonate and 0.5 g of cupric chloride dihydrate. The mixture was gradually warmed up to room temperature and stirred at room temperature for 2 hours. Acetone was evaporated off and the residue was extracted with ether. The ether layer was washed with water and dried over anhydrous magnesium sulfate and the solvent was evaporated off. The residue thus obtained was subjected to silica gel column chromatography (eluent: ethyl acetate--dioxane--n-hexane=1:1:4) and recrystallized from n-hexane to obtain 2.3 g of 2-[3-fluoro-4-(2,2,2-trichloroethyl)phenyl]propionic acid, m.p. 92°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04557871
Source datasetuspto-grants-1985_12
ORD IDord-5b5518fb236e4e70898d154651973337
Source noteuspto-grants-1985_12