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HRID 131184作成日:2026年10月25日

Triphenylphosphane dibromide → (2S)-4-Benzyl-2-[bromo(phenyl)methyl]morpholine

https://huagongshe.com/reaction/131184

反応式

関与物質

役割名称HCID仕込み量
反応物Triphenylphosphane dibromideHCID 12890784—
反応物(S)-Phenyl[(2S)-4-(phenylmethyl)morpholin-2-yl]methanolHCID 58997981—
溶媒ChloroformHCID 6212—
生成物(2S)-4-Benzyl-2-[bromo(phenyl)methyl]morpholineHCID 5899797981%

反応条件

温度60 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384941B2
出典データセットuspto-grants-2008_06
ORD IDord-a1606e5abd05412897a62fe2d03a68d4
出典メモuspto-grants-2008_06