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Chloroacetyl chloride → HCID 11107745, 화합물

HRID 232704
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HRID 232704 반응식
[Cl:1][CH2:2][C:3](Cl)=[O:4].[Cl-].[Al+3].[Cl-].[Cl-].[CH2:10]([C:12]1[CH:13]=[CH:14][CH:15]=[C:16]2[C:21]=1[NH:20][C:19](=[O:22])[CH:18]=[CH:17]2)[CH3:11]>C(=S)=S>[Cl:1][CH2:2][C:3]([C:14]1[CH:15]=[C:16]2[C:21](=[C:12]([CH2:10][CH3:11])[CH:13]=1)[NH:20][C:19](=[O:22])[CH:18]=[CH:17]2)=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6577Chloroacetyl chlorideHCID 6451240Aluminum(III) ChlorideHCID 108668132(1H)-Quinolinone, 8-ethyl-

생성물 1

HCID 11107745HCID 11107745, 화합물

시약·촉매·용매 1

HCID 6348Carbon Disulfide용매

실험 절차

To a solution of 62 ml of chloroacetyl chloride in 600 ml of carbon disulfide were added, with ice-cooling, 173 g of aluminum chloride and 44 g of 8-ethylcarbostyril in this order. The mixture was refluxed for 6 hours. The reaction mixture was subjected to distillation to remove carbon disulfide. The residue was poured into ice water. The mixture was stirred at room temperature overnight. The insoluble portion was collected by filtration, washed with water and dried to obtain 55 g of 6-chloroacetyl-8-ethylcarbostyril as a brown powder.

후처리

  1. temperaturecooling
  2. temperatureThe mixture was refluxed for 6 hours
  3. distillationThe reaction mixture was subjected to distillation
  4. customto remove carbon disulfide
  5. additionThe residue was poured into ice water
  6. filtrationThe insoluble portion was collected by filtration
  7. washwashed with water
  8. customdried

출처 및 근거

ORD 기록
ord-379c6a31a2e94220a350956cae039110
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05591751

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