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openreactiondata ↗doi:10.1039/C8SC04228D
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来源 ID: ord-2918e1fe47284303b22a891efc1b3d2a暂无可渲染的结构数据
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12 条反应 · 12 篇文献
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来源 ID: ord-3407a331034e4ed88152bcc27194c263反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Tetrabutylammonium fluoride (0.1 ml; 1.0 M solution in tetrahydrofuran) was added to a solution of 2-trifluoromethyl-benzaldehyde (1.74 g, 10 mmol) and trifluoromethyltrimethylsilane (TMSCF3) (1.8 ml, 12 mmol) in 10 ml THF at 0° C. The formed mixture was warmed up to room temperature and stirred for 4 hours. The reaction mixture was then treated with 12 ml of 1N 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 2.2 g of 1-(2-trifluoromethylphenyl)-2,2,2-trifluoro-ethanol, yield 90%. stirred overnight The product was extracted with ethyl acetate (3×20 ml) The organic layer was separated dried over sodium sulfate The organic solvent was evaporated
来源 ID: ord-97d12a6e1e544737a489e32b68b7067aPubChem References
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