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Hydrogen Bromide → 1-(3-bromopropyl)-5,6-dichloro-1,3-dihydro-2H-benzimidazol-2-one

HRID 126848
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HRID 126848 반응식
[Cl:1][C:2]1[C:15]([Cl:16])=[CH:14][C:5]2[N:6]([CH2:10][CH2:11][CH2:12]O)[C:7](=[O:9])[NH:8][C:4]=2[CH:3]=1.[BrH:17]>O>[Br:17][CH2:12][CH2:11][CH2:10][N:6]1[C:5]2[CH:14]=[C:15]([Cl:16])[C:2]([Cl:1])=[CH:3][C:4]=2[NH:8][C:7]1=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 202880345,6-dichloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one

생성물 1

HCID 202880671-(3-bromopropyl)-5,6-dichloro-1,3-dihydro-2H-benzimidazol-2-one수율 81%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

A mixture of 57.5 parts of 5,6-dichloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one and 450 parts of a hydrobromic acid solution 48% in water is stirred and refluxed for 2.50 hours. The reaction mixture is cooled and water is added. The precipitated product is filtered off, stirred in 700 parts of water, filtered off again and dried in vacuo, yielding 59 parts (81%) of 1-(3-bromopropyl)-5,6-dichloro-1,3-dihydro-2H-benzimidazol-2-one; mp. 198.1° C.

후처리

  1. temperaturerefluxed for 2.50 hours
  2. temperatureThe reaction mixture is cooled
  3. filtrationThe precipitated product is filtered off
  4. stirringstirred in 700 parts of water
  5. filtrationfiltered off again
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-af68619533ab484c9d2788f36e347762
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04254127

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