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

HRID 1153977
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HRID 1153977 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane
용매

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온도
0 °C

실험 절차

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. Colorless needle-like crystals. Melting point: 90°-92° C.

후처리

  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

출처 및 근거

ORD 기록
ord-62199e5afa814648bce5587d540a3508
출처 데이터셋
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04487772

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