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Chloroacetyl chloride → HCID 14143058、化合物

HRID 1366680
ノート
印刷プレビュー

反応式

HRID 1366680 の反応式
[C:1]1([CH2:7][NH:8][C@@H:9]([CH3:12])[CH2:10][OH:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([O-])([O-])=O.[K+].[K+].Cl[CH2:20][C:21](Cl)=[O:22].[OH-].[Na+]>C1COCC1.O>[CH3:12][C@@H:9]1[N:8]([CH2:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)[C:21](=[O:22])[CH2:20][O:11][CH2:10]1
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

7

反応物 4

HCID 6577Chloroacetyl chloride2 回HCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 5356540N-Benzyl-L-alaninol

生成物 1

HCID 14143058HCID 14143058、化合物収率 97.5%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
0 °C

実験手順

To a solution of (2S)-2-[(phenylmethyl)amino]-1-propanol (10.52 g, 63.67 mmol) in THF (65 mL) was added a solution of K2CO3 (26.40 g, 191.0 mmol) in water (65 mL). The vigorously stirred mixture was cooled to 0° C., and chloroacetyl chloride (7.10 mL, 89.14 mmol) was added dropwise over 20 min. The mixture was stirred for 1 h, and then an additional portion of chloroacetyl chloride (0.500 mL, 6.278 mmol) was added dropwise. The mixture was stirred for 1 h, and then the mixture was adjusted to pH>13 with 50% aq. NaOH (ca. 20 mL). The mixture was stirred and warmed to room temperature overnight, and then extracted with DCM (250 mL). The organic phase was washed with 1 N aq. HCl, followed by water. The organic phase was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to give (5S)-5-methyl-4-(phenylmethyl)-3-morpholinone (12.74 g, 97%) as a colorless oil. LCMS: (M+H)+: 206.1.

後処理

  1. stirringThe mixture was stirred for 1 h
  2. stirringThe mixture was stirred
  3. temperaturewarmed to room temperature overnight
  4. extractionextracted with DCM (250 mL)
  5. washThe organic phase was washed with 1 N aq. HCl
  6. dry with materialThe organic phase was dried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-4b2d8f3e79f0433e852c6be9bdde715c
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07893056B2

反応ノート

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