反応式
[C:1]([NH2:5])([CH3:4])([CH3:3])[CH3:2].[Cl:6][CH2:7][CH2:8][CH2:9][S:10](Cl)(=[O:12])=[O:11]>C1COCC1>[C:1]([NH:5][S:10]([CH2:9][CH2:8][CH2:7][Cl:6])(=[O:12])=[O:11])([CH3:4])([CH3:3])[CH3:2]参加物
4
反応条件
- 温度
- -20 °C
実験手順
tert-Butylamine (3.0 mol, 315.3 mL) was dissolved in THF (2.5 L). The solution was cooled to −20° C. 3-Chloropropanesulfonyl chloride (1.5 mol, 182.4 mL) was added slowly. The reaction mixture was allowed to warm to rt and stirred for 24 h. The mixture was filtered, and the filtrate was concentrated in vacuo. The residue was dissolved in CH2Cl2 (2.0 L). The resulting solution was washed with 1 N HCl (1.0 L), water (1.0 L), brine (1.0 L) and dried over Na2SO4. It was filtered and concentrated in vacuo to give a slightly yellow solid, which was crystallized from hexane to afford the product as a white solid (316.0 g, 99%).
後処理
- temperatureto warm to rt
- filtrationThe mixture was filtered
- concentrationthe filtrate was concentrated in vacuo
- dissolutionThe residue was dissolved in CH2Cl2 (2.0 L)
- washThe resulting solution was washed with 1 N HCl (1.0 L), water (1.0 L), brine (1.0 L)
- dry with materialdried over Na2SO4
- filtrationIt was filtered
- concentrationconcentrated in vacuo
- customto give a slightly yellow solid, which
- customwas crystallized from hexane
出典と根拠
- ORDレコード
- ord-4d152abc044543a395564c614ea0d57a
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07741281B2
関連ノート
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