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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260511Generated: October 26, 2026

Hydrochloric Acid → 1-[4-(Trifluoromethyl)phenyl]propan-1-ol

https://huagongshe.com/reaction/2260511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantEthyl BromideHCID 6332—
Reactant4-(Trifluoromethyl)benzaldehydeHCID 67996—
ReactantMagnesiumHCID 5462224—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-[4-(Trifluoromethyl)phenyl]propan-1-olHCID 5314415—

Reaction Conditions

Temperature0 °C

Reaction Steps

Dry tetrahydrofuran (700 mL), magnesium turnings (16.75 g, 0.69 mol, 1.2 eq), and a iodine crystal were placed in a flask and the mixture was stirred intensively at 0° C. Bromoethane (68 g, 46.7 mL, 0.69 mol, 1.1 eq) was added dropwise and the resulting mixture was allowed to stir for 30 min. Then the reaction mixture was treated with 4-trifluoromethylbenzaldehyde (100 g, 0.57 mol, 1 eq). After stirring at room temperature for 2 h, the reaction mixture was cooled to 0° C. and poured carefully to a mixture of 1N HCl (750 mL) and ice cooled to 0° C. and poured carefully to a mixture of 1N HCl (750 mL) and ice with CH2Cl2. The organic layer was washed with 5% aqueous NaHCO3 and with CH2Cl2. The organic layer was washed with 5% aqueous NaHCO3 and brine, then dried over anhydrous Na2SO4, the drying agent was filtered and

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478826
Source datasetuspto-grants-1995_12
ORD IDord-f75a90d5b5e3410fab6666f3d7a61c02
Source noteuspto-grants-1995_12