Hydroxylamine → Benzyl hydroxycarbamate
反応式
[NH2:1][OH:2].C([O-])([O-])=O.[K+].[K+].Cl[C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11]>C(Cl)Cl>[C:10]([NH:1][OH:2])([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[O:11]参加物
5
実験手順
A solution of crude amino alcohol 1f (223 g, 1.19 mol) in 1 L of CH2Cl2 was treated with a 1 L aqueous solution of K2CO3 (200 g, 1.45 mol) and cooled in a ice bath. The mixture is stirred vigorously while benzyl chloroformate (225 g, 1.3 mol) is added slowly. After the addition is complete the mixture is stirred an additional 30 min. The organic layer is separated and washed with water, brine and concentrated to give 390 g of crude product. This is recrystallized from hexane to give 270 g of N-CBZ amino alcohol 1 g.
後処理
- temperaturecooled in a ice bath
- additionis added slowly
- additionAfter the addition
- customThe organic layer is separated
- washwashed with water, brine
- concentrationconcentrated
- customto give 390 g of crude product
- customThis is recrystallized from hexane
出典と根拠
- ORDレコード
- ord-485bca5cd3f948ba9ce67e774ca138bd
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07351720B2
反応ノート
読み込み中…