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Chloroacetyl chloride → Benzenepropanoic acid, 4-(chloroacetyl)-, methyl ester

HRID 1262840
ノート
印刷プレビュー

反応式

HRID 1262840 の反応式
[C:1]1([CH2:7][CH2:8][C:9]([O:11][CH3:12])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:13][CH2:14][C:15](Cl)=[O:16].[Cl-].[Al+3].[Cl-].[Cl-].C(OC(C)C)(C)C>ClCCl>[Cl:13][CH2:14][C:15]([C:4]1[CH:5]=[CH:6][C:1]([CH2:7][CH2:8][C:9]([O:11][CH3:12])=[O:10])=[CH:2][CH:3]=1)=[O:16]
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

6

反応物 4

HCID 6577Chloroacetyl chlorideHCID 7643Methyl 3-phenylpropionateHCID 7914Diisopropyl EtherHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 10800114Benzenepropanoic acid, 4-(chloroacetyl)-, methyl ester収率 72.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane
溶媒

反応条件

温度
0 °C

実験手順

A mixture of 50 g of methyl 3-phenylpropionate, 51.6 g of chloroacetyl chloride and 250 ml of dichloromethane was cooled to 0° C. Then at 0° to 10° C. with stirring, 122 g of aluminum chloride was added slowly, stirred at a room temperature for 2 hours and allowed to stand overnight. The reaction mixture was poured into an ice-concentrated hydrochloric acid and extracted with chloroform, then the chloroform layer was washed with water, dried and the chloroform was removed by distillation to obtain the residue, then isopropyl ether was added to the residue to effect crystallization. The crystals were collected by filtration, and recrystallized from ethanol to obtain 53.4 g of methyl 3-(4-chloroacetylphenyl)-propionate.

後処理

  1. stirringstirred at a room temperature for 2 hours
  2. extractionextracted with chloroform
  3. washthe chloroform layer was washed with water
  4. customdried
  5. customthe chloroform was removed by distillation
  6. customto obtain the residue
  7. customcrystallization
  8. filtrationThe crystals were collected by filtration
  9. customrecrystallized from ethanol

出典と根拠

ORDレコード
ord-a1ecda2a867849f3b91361e9cb4512c0
出典データセット
uspto-grants-1984_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04454130

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート