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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625874Generated: October 30, 2026

Tetrahydrofuran → 5-Bromo-1-(5-phenyl-2-thienylmethyl)-2-trifluoromethylbenzene

https://huagongshe.com/reaction/1625874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Bromo-2-trifluoromethylphenyl 5-phenyl-2-thienyl ketoneHCID 66608925—
SolventMethanolHCID 887—
Product5-Bromo-1-(5-phenyl-2-thienylmethyl)-2-trifluoromethylbenzeneHCID 6660689087.3%

Reaction Steps

To a mixed solution of the above 5-bromo-2-trifluoromethylphenyl 5-phenyl-2-thienyl ketone (670 mg) in methanol (20 ml)-tetrahydrofuran (10 ml) was added sodium borohydride (62 mg), and the mixture was stirred at room temperature for 3 hours. The solvent was evaporated under reduced pressure, and the residue was dissolved in chloroform (10 ml)-acetonitrile (20 ml). Thereto was added triethylsilane (0.78 ml), and the mixture was cooled to 0° C. Thereto was added dropwise boron trifluoride.diethyl ether complex (0.52 ml). The mixture was stirred at room temperature for 45 minutes, and added thereto was a saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane) to give the desired 5-bromo-1-(5-phenyl-2-thienylmethyl)-2-trifluoromethylbenzene (565 mg) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-75b1130cbfcc427498664511a4c837e5
Source noteuspto-grants-2014_07