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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755036Generated: October 28, 2026

Hydrochloric Acid → HCID 59987958, compound

https://huagongshe.com/reaction/1755036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 4-FormylbenzoateHCID 15294—
ReactantSodium BicarbonateHCID 516892—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
CatalystPotassium AcetateHCID 517044—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59987958HCID 5998795895.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

DMF (10 mL) was added to a reaction vessel containing 4-formyl-benzoic acid methyl ester (501.1 mg, 3.053 mmol) and potassium acetate (15.0 mg, 0.153 mmol), and the mixture was cooled to 0° C. Trimethyl(trifluoromethyl)silane (0.96 mL, 6.105 mmol) was added dropwise and the mixture was stirred for 50 minutes. 2 N hydrochloric acid (10 mL) was then added to the reaction mixture, and the mixture was stirred at room temperature overnight and then diluted with ethyl acetate. A saturated aqueous sodium bicarbonate solution was added, and the organic layer and the aqueous layer were separated. The organic layer was sequentially washed with water and saturated brine, and then dried over anhydrous Na2SO4 and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to give 4-(2,2,2-trifluoro-1-hydroxy-ethyl)-benzoic acid methyl ester (680.8 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-8255ad144fdd4e6980833baca9cf229f
Source noteuspto-grants-2015_10