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HRID 1620872作成日:2026年10月25日

Hydrochloric Acid → 2,2,2-Trifluoro-1-(2-furan-3-yl-phenyl)-ethanol

https://huagongshe.com/reaction/1620872

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TetrahydrofuranHCID 8028—
反応物(Trifluoromethyl)trimethylsilaneHCID 552549—
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物2-(Furan-2-yl)benzaldehydeHCID 2772294—
生成物2,2,2-Trifluoro-1-(2-furan-3-yl-phenyl)-ethanolHCID 6674368890%

反応手順

Tetrabutylammonium fluoride (0.1 ml of 1M in THF) was added to a solution of 2-furan-2-yl-benzaldehyde (123 mg, 0.71 mmol) and trifluoromethyl trimethylsilane (120 mg, 0.86 mmol) in 10 ml THF at 0° C. The mixture was warmed up to room temperature and stirred for 4 hours. The reaction mixture was then treated with 3 ml of 1M HCl and stirred overnight. The product was extracted with ethyl acetate (3×20 ml). The organic layer was separated and dried over sodium sulfate. The organic solvent was evaporated to give 0.150 g of 2,2,2-trifluoro-1-(2-furan-3-yl-phenyl)-ethanol, which was directly used in next step without purification (yield: 90%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08772482B2
出典データセットuspto-grants-2014_07
ORD IDord-a82c51f96dc34ffb85df9797f9b72cc8
出典メモuspto-grants-2014_07