Potassium Hydroxide → 4-Difluoromethoxy-piperidine
反応式
[F:1][CH:2]([F:12])[O:3][CH:4]1[CH2:9][CH2:8][N:7](C=O)[CH2:6][CH2:5]1.[OH-].[K+]>O>[F:1][CH:2]([F:12])[O:3][CH:4]1[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1参加物
4
実験手順
4-(difluoromethoxy)piperidine-1-carbaldehyde (17) (2.7 g, 15.07 mmol) and potassium hydroxide (2.96 g, 52.74 mmol) were dissolved in water (40 mL) and stirred vigorously for 3 hours. The reaction was extracted with diethyl ether (3×75 mL), the organic layer was dried over MgSO4, filtered and evaporated to afford an orange liquid. The crude product was purified by distillation at 0.70 mBar, collecting fractions that distilled at 25° C. to afford the desired material as a colourless oil (1.100 g, 48.3%); 1H NMR (400.132 MHz, CDCl3) δ 1.50 (1H, s), 1.66-1.57 (2H, m), 1.95-1.89 (2H, m), 2.70-2.64 (2H, m), 3.09 (2H, dt), 4.25-4.19 (1H, m), 6.24 (1H, t).
後処理
- extractionThe reaction was extracted with diethyl ether (3×75 mL)
- dry with materialthe organic layer was dried over MgSO4
- filtrationfiltered
- customevaporated
- customto afford an orange liquid
- distillationThe crude product was purified by distillation at 0.70 mBar
- customcollecting fractions
- distillationthat distilled at 25° C.
出典と根拠
- ORDレコード
- ord-1f0d51340769469894af7fb14d2d5fb6
- 出典データセット
- uspto-grants-2012_03
- 特許番号
- US08129380B2
反応ノート
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