Triphosgene → [(1S)-1-isocyanatopropyl]benzene
反応式
[C:1]1([C@@H:7]([NH2:10])[CH2:8][CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:11]([O-])(O)=[O:12].[Na+].ClC(Cl)(OC(=O)OC(Cl)(Cl)Cl)Cl>C(Cl)Cl>[N:10]([C@H:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[CH2:8][CH3:9])=[C:11]=[O:12]参加物
5
実験手順
To a solution of (S)-1-phenylpropan-1-amine (3.00 g, 14 mmol) in the mixture of methylene chloride (50 mL) and saturated NaHCO3 (50 mL) was added triphosgene (1.40 g, 4.60 mmol) at 0° C. The mixture was stirred for 15 minutes. The organic phase was separated, dried and concentrated to give (S)-(1-isocyanatopropyl)benzene (3.0 g, 88%). 1H NMR (CDCl3): δ=0.93 (q, 3H), 1.81 (m, 2H), 4.50 (m, 1H), 7.13 (m, 2H), 7.22 (m, 1H), 7.50 (m, 2H).
後処理
- customThe organic phase was separated
- customdried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-4e09c8a2083e4ec1b2f69852401c0e40
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08487094B2
反応ノート
読み込み中…