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Thionyl Chloride → [Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester

HRID 1912426
ノート
印刷プレビュー

反応式

HRID 1912426 の反応式
[C:1]([O:5][C:6](=[O:20])[CH2:7][N:8]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH:9]([CH3:12])[CH2:10]O)([CH3:4])([CH3:3])[CH3:2].S(Cl)([Cl:23])=O.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl>[C:1]([O:5][C:6](=[O:20])[CH2:7][N:8]([CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH:9]([CH3:12])[CH2:10][Cl:23])([CH3:4])([CH3:3])[CH3:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24386Thionyl ChlorideHCID 516892Sodium BicarbonateHCID 58293285[Benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl ester

生成物 1

HCID 58293349[Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒2 回

反応条件

温度
60 °C

実験手順

To a solution of an optically-active compound of [benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl ester (160.0 g) in chloroform (640 ml) cooled to 0° C. was added dropwise thionyl chloride (50.0 ml), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was cooled to 0° C. Then, thereto were added saturated aqueous sodium bicarbonate solution (1000 ml) and chloroform (100 ml), and the mixture was stirred. The separated organic layer was washed with saturated aqueous sodium chloride solution (500 ml), and the aqueous layer was extracted with chloroform (450 ml) again. The combined organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the titled compound (172.9 g).

後処理

  1. temperatureThe reaction mixture was cooled to 0° C
  2. stirringthe mixture was stirred
  3. washThe separated organic layer was washed with saturated aqueous sodium chloride solution (500 ml)
  4. extractionthe aqueous layer was extracted with chloroform (450 ml) again
  5. dry with materialThe combined organic layer was dried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-4197bcef3b754de489e2486bb8ec9e1a
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08609647B2

反応ノート

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