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Aniline → 3-(Phenylsulfamoyl)benzoic acid

HRID 2308278
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HRID 2308278 반응식
Cl[S:2]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=1)[C:8]([OH:10])=[O:9])(=[O:4])=[O:3].[NH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(Cl)Cl>[C:15]1([NH:14][S:2]([C:5]2[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=2)[C:8]([OH:10])=[O:9])(=[O:4])=[O:3])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
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참가 물질

4

반응물 2

HCID 6115AnilineHCID 77641Benzoic acid, 3-(chlorosulfonyl)-

생성물 1

HCID 7593393-(Phenylsulfamoyl)benzoic acid수율 100.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3-Chlorosulfonyl-benzoic acid (300 mg, 1.36 mmol), and aniline (0.30 mL, 3.29 mmol) were stirred at room temperature in anhydrous CH2Cl2 (10 mL) overnight under N2. The reaction mixture was concentrated in vacuo. Purification of the residue on IR-120 ion exchange resin column (eluted with methanol) afforded the title compound (380 mg, 100%) as a white solid.

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customPurification of the residue
  3. washon IR-120 ion exchange resin column (eluted with methanol)

출처 및 근거

ORD 기록
ord-e4d6ccb5ae8a413991c3c0f0c0194871
출처 데이터셋
uspto-grants-2004_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06835731B2

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