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Water → N,N-Dimethyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide

HRID 1840330
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HRID 1840330 반응식
[CH3:1][N:2]([CH3:17])[S:3]([C:6]1[C:11]([Cl:12])=[CH:10][CH:9]=[C:8]([N+:13]([O-:15])=[O:14])[C:7]=1Cl)(=[O:5])=[O:4].[H-].[Na+].[OH2:20]>>[CH3:1][N:2]([CH3:17])[S:3]([C:6]1[C:11]([Cl:12])=[CH:10][CH:9]=[C:8]([N+:13]([O-:15])=[O:14])[C:7]=1[OH:20])(=[O:5])=[O:4]
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참가 물질

4

반응물 3

HCID 962WaterHCID 24758Sodium hydrideHCID 23447825N,N-Dimethyl-2,6-dichloro-3-nitrobenzenesulfonamide

생성물 1

HCID 23447760N,N-Dimethyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide수율 93%

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온도
35 °C

실험 절차

A mixture of N,N-dimethyl-2,6-dichloro-3-nitrobenzenesulfonamide (2.64 g, 8.83 mmol), 60% sodium hydride (1.06 g, 26.5 mmol) and water (191 mg, 10.6 mmol) was heated to 35° C. while kept under argon atmosphere for 16 hours. The solvent was evaporated. when The reaction was almost complete as indicated by 1H NMR. The residue was diluted with ethyl acetate and washed with 1N aq. HCl. The solvent was concentrated to give the crude material. Column chromatography on silica gel, eluting with ethyl acetate/hexane/acetic acid (40/58/2, v/v/v), gave the desired product (2.3 g, 93%). EI-MS (m/z)279.5 (M−).

후처리

  1. customThe solvent was evaporated
  2. additionThe residue was diluted with ethyl acetate
  3. washwashed with 1N aq. HCl
  4. concentrationThe solvent was concentrated
  5. customto give the crude material
  6. washColumn chromatography on silica gel, eluting with ethyl acetate/hexane/acetic acid (40/58/2, v/v/v)

출처 및 근거

ORD 기록
ord-685d8de857934db0b0911c0c18b601ee
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06680317B2

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