反応式
[F:1][C:2]([F:13])([F:12])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=O>C1COCC1>[F:1][C:2]([F:12])([F:13])[CH2:3][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1参加物
3
実験手順
To a solution of 2,2,2-trifluoro-N-phenylacetamide (5.0 g, 26 mmol) in THF (10 mL) was added BH3 in THF (130 mL, 130 mmol, 1.0 M). The resulting mixture was refluxed overnight. The mixture was quenched with water and methanol, concentrated to remove most of THF, and extracted with EtOAc. Organics were washed with brine, dried (Na2SO4), and concentrated to give 4.17 g (92%) of the title compound as a colorless oil. 1H NMR (400 MHz, CDCl3): δ 3.71-3.75 (2H, m), 6.66 (2H, d, J=8.0 Hz), 6.79 (1H, t, J=7.2 Hz), 7.20 (2H, t, J=8.0 Hz).
後処理
- temperatureThe resulting mixture was refluxed overnight
- customThe mixture was quenched with water and methanol
- concentrationconcentrated
- customto remove most of THF
- extractionextracted with EtOAc
- washOrganics were washed with brine
- dry with materialdried (Na2SO4)
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-5dbcc5a4847a4c849cb9ac0248c9d91c
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447046B2
関連ノート
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