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Hydrogen Bromide → 2-Bromo-5-chloro-6-n-propylsulfamoyl-1-indanone

HRID 65935
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반응식

HRID 65935 반응식
[BrH:1].[Cl:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[S:12](=[O:18])(=[O:17])[NH:13][CH2:14][CH2:15][CH3:16])[C:8](=[O:19])[CH2:7][CH2:6]2.BrBr>C(OCC)(=O)C>[Br:1][CH:7]1[CH2:6][C:5]2[C:9](=[CH:10][C:11]([S:12](=[O:17])(=[O:18])[NH:13][CH2:14][CH2:15][CH3:16])=[C:3]([Cl:2])[CH:4]=2)[C:8]1=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 260Hydrogen BromideHCID 24408BromineHCID 227563895-Chloro-6-n-propylsulfamoyl-1-indanone

생성물 1

HCID 227563962-Bromo-5-chloro-6-n-propylsulfamoyl-1-indanone

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매2회

실험 절차

0.5 L Milliliter of 48% aqueous HBr is added to a solution of 5.76 g (20 mmoles) of 5-chloro-6-n-propylsulfamoyl-1-indanone in 50 ml of ethyl acetate. Thereafter a solution of 3.20 g (20 mmoles) of bromine in 20 ml of ethyl acetate is added dropwise. The mixture is stirred for 1 hour at room temperature, then the solution is concentrated to dryness, and 50 ml of water are added to the residue. The crystalline precipitate is filtered off with suction and washed with water. 2-Bromo-5-chloro-6-n-propylsulfamoyl-1-indanone is obtained which has a melting point of from 150° to 154° C.

후처리

  1. concentrationthe solution is concentrated to dryness, and 50 ml of water
  2. additionare added to the residue
  3. filtrationThe crystalline precipitate is filtered off with suction
  4. washwashed with water

출처 및 근거

ORD 기록
ord-5d4b4141148a4dc3bec6d7144c954f6c
출처 데이터셋
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04129656

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