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p-Toluenesulfonic acid monohydrate → HCID 136335909, 화합물

HRID 2266439
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인쇄 미리보기

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HRID 2266439 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[CH:6][C:7]=1[Cl:8].[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([S:17][CH:18]([C:22](=O)[CH3:23])[C:19](=O)[CH3:20])=[CH:13][CH:12]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[Cl:8][C:7]1[C:2]2[N:1]=[C:22]([CH3:23])[C:18]([S:17][C:14]3[CH:13]=[CH:12][C:11]([Cl:10])=[CH:16][CH:15]=3)=[C:19]([CH3:20])[C:3]=2[C:4]([OH:9])=[CH:5][CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 521998p-Toluenesulfonic acid monohydrateHCID 7226463-[(4-Chlorophenyl)thio]pentane-2,4-dioneHCID 50700783-Amino-4-chlorophenol

생성물 1

HCID 136335909HCID 136335909, 화합물

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온도
140 °C

실험 절차

A mixture of 3-amino-4-chlorophenol (0.36 g), 3-(4-chlorophenylsulfanyl)pentane-2,4-dione (0.61 g) and p-toluenesulfonic acid monohydrate (0.040 g) was heated at 140° C. for 10 hours. The mixture was cooled to room temperature and purified by column chromatography on silica gel, eluting with a mixture of dichloromethane and ethyl acetate (1:0 to 0:1 by volume) to afford title compound as a brown oil, 0.050 g.

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. custompurified by column chromatography on silica gel
  3. washeluting with a mixture of dichloromethane and ethyl acetate (1:0 to 0:1 by volume)

출처 및 근거

ORD 기록
ord-0c9463967f214b2590df8a3b07492469
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07858640B2

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