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Hydrochloric Acid → 2-(1-Piperazinyl)-5-propylbenzenesulfonic acid hydrochloride

HRID 344663
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인쇄 미리보기

반응식

HRID 344663 반응식
[ClH:1].[N:2]1([C:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH3:16])=[CH:10][C:9]=2[S:17]([OH:20])(=[O:19])=[O:18])[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1>C(O)C>[ClH:1].[N:2]1([C:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][CH3:16])=[CH:10][C:9]=2[S:17]([OH:20])(=[O:18])=[O:19])[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 30273132-(1-Piperazinyl)-5-n-propylbenzenesulfonic acid

생성물 1

HCID 30273122-(1-Piperazinyl)-5-propylbenzenesulfonic acid hydrochloride수율 95.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a mixed solution of 200 ml of ethyl alcohol and 185 ml of 1 N hydrochloric acid was added 50.0 g of 2-(1-piperazinyl)-5-n-propylbenzenesulfonic acid and the mixture was dissolved by heating. The mixture was condensed under reduced pressure, and precipitated crystals were washed with acetone and dried to give 51.46 g (yield: 95.4%) of the above title product.

후처리

  1. dissolutionthe mixture was dissolved
  2. temperatureby heating
  3. customcondensed under reduced pressure
  4. customprecipitated crystals
  5. washwere washed with acetone
  6. customdried

출처 및 근거

ORD 기록
ord-d76cb509ad854474bc39f92d9a615bb1
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05053409

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