反応式
Br[CH2:2][C:3](Cl)=[O:4].C1(C)C=CC=CC=1.[OH-].[Na+].[NH2:15][C@@H:16]([CH2:19][O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH2:17][OH:18]>C1COCC1>[CH2:21]([O:20][CH2:19][C@@H:16]1[NH:15][C:3](=[O:4])[CH2:2][O:18][CH2:17]1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1参加物
反応条件
- 温度
- 0 °C
実験手順
Bromoacetyl chloride (5.06 mL) was added to a solution mixture of toluene (100 mL) and a 2 N sodium hydroxide aqueous solution (100 mL) of (R)-(+)-2-amino-3-benzyloxy-1-propanol (10 g) under ice-cooling. The resulting reaction solution was stirred at 0° C. for 30 min and then further stirred at 60° C. for 1 hr. The reaction solution was cooled to room temperature, and a solution mixture of toluene and THF (1:1) was added thereto. The organic layer was separated, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system) to give 1.36 g of the title compound. The physical property values of this compound were as follows:
後処理
- customThe resulting reaction solution
- stirringfurther stirred at 60° C. for 1 hr
- temperatureThe reaction solution was cooled to room temperature
- additionwas added
- customThe organic layer was separated
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was purified by silica gel column chromatography (eluting solvent: heptane-ethyl acetate system)
出典と根拠
- ORDレコード
- ord-0de979c1ecc44607a3376da65e857d14
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07737141B2
関連ノート
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