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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Bromo-2-trifluoromethylphenyl 5-phenyl-2-thienyl ketone | HCID 66608925 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-1-(5-phenyl-2-thienylmethyl)-2-trifluoromethylbenzene | HCID 66606890 | 87.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785403B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-75b1130cbfcc427498664511a4c837e5 |
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| Source note | uspto-grants-2014_07 |
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