関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triphenylphosphane dibromide | HCID 12890784 | — |
| 反応物 | (S)-Phenyl[(2S)-4-(phenylmethyl)morpholin-2-yl]methanol | HCID 58997981 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | (2S)-4-Benzyl-2-[bromo(phenyl)methyl]morpholine | HCID 58997979 | 81% |
反応手順
To a solution of 4a (4.71 g, 16.6 mmol) in anhydrous chloroform (200 ml) under nitrogen was added triphenylphosphine dibromide (14.04 g, 33.26 mmol). The reaction mixture was heated at 60° C. overnight. The mixture was allowed to cool to room temperature then washed with saturated aqueous sodium carbonate solution, dried over sodium sulphate and concentrated in vacuo. The resulting residue was purified by flash chromatography on silica (eluent: ethyl acetate/isohexane gradient 10/90 to 30/70 [v/v]) to give 5a as a white solid (4.63 g, 81%); MW 346.27; C18H20BrNO; 1H NMR (CDCl3): 7.14-7.39 (10H, m), 4.83 (1H, d, 7 Hz), 4.01 (1H, br, t, 8 Hz), 3.73 (1H, br, d, 11 Hz), 3.60-3.48 (2H, m), 3.39 (1H, d, 12 Hz), 3.20 (1H, d, 11 Hz), 2.50 (1H, d, 10 Hz), 2.07 (2H, t, 10 Hz); LCMS: (6 min method) m/z 346 [M]+ @ Rt 2.51 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07384941B2 |
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| 出典データセット | uspto-grants-2008_06 |
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| ORD ID | ord-a1606e5abd05412897a62fe2d03a68d4 |
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| 出典メモ | uspto-grants-2008_06 |
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