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Thionyl Chloride → 4-Isopropyl-3-sulfamoylbenzoylchloride

HRID 1703889
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인쇄 미리보기

반응식

HRID 1703889 반응식
[CH:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8](O)=[O:9])=[CH:6][C:5]=1[S:13](=[O:16])(=[O:15])[NH2:14])([CH3:3])[CH3:2].S(Cl)([Cl:19])=O>>[CH:1]([C:4]1[CH:12]=[CH:11][C:7]([C:8]([Cl:19])=[O:9])=[CH:6][C:5]=1[S:13](=[O:16])(=[O:15])[NH2:14])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 167729934-(Propan-2-yl)-3-sulfamoylbenzoic acid

생성물 1

HCID 227605054-Isopropyl-3-sulfamoylbenzoylchloride

실험 절차

5 g of 4-isopropyl-3-sulfamoylbenzoic acid were boiled under reflux in 50 ml of thionylchloride until completely dissolved and the reaction mixture was then concentrated to 25 ml under reduced pressure. After allowing to dwell over night at 0° C., the crystals were filtered off over a sinter glass frit and washed with petroleum ether. Colorless body, melting point: 177° C.

후처리

  1. dissolutionuntil completely dissolved
  2. concentrationthe reaction mixture was then concentrated to 25 ml under reduced pressure
  3. waitto dwell over night at 0° C.
  4. filtrationthe crystals were filtered off over a sinter glass frit
  5. washwashed with petroleum ether

출처 및 근거

ORD 기록
ord-23b4c0f88371407fafbfe72f8afdade4
출처 데이터셋
uspto-grants-1978_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04125614

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