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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253374Generated: November 2, 2026

Hydrochloric Acid → 3-(Trifluoromethyl)benzenepropanal

https://huagongshe.com/reaction/1253374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylaluminium hydrideHCID 21896610—
ReactantMethyl 3-[3-(trifluoromethyl)phenyl]propanoateHCID 53230361—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product3-(Trifluoromethyl)benzenepropanalHCID 11298612101.5%

Reaction Steps

2.40 g of 3-(3-trifluoromethylphenyl)-propionic acid methyl ester synthesized in Step 1 was dissolved in 20 ml of dry dichloromethane. 13 ml of diisopropyl aluminum hydride solution (0.91 M) in hexane was dropped over 5 minutes at −78° C. under an argon atmosphere, and the mixture was stirred at the same temperature for 40 minutes. 50 ml of a saturated ammonium chloride aqueous solution was dropped, and then the mixture was stirred and the temperature was raised to room temperature. 20 ml of water and 5 ml of concentrated hydrochloric acid were added, and the resultant was separated into an aqueous layer and an organic layer. The aqueous layer was extracted with dichloromethane, and the extract was combined with the separated organic layer, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to afford 2.12 g of the captioned compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08454978B2
Source datasetuspto-grants-2013_06
ORD IDord-64c890373e31474e8e3db64fe1117611
Source noteuspto-grants-2013_06