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2-Nitrobenzenesulfonyl chloride → N-(Benzyloxy)-2-nitrobenzenesulfonamide

HRID 515586
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HRID 515586 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10](Cl)(=[O:12])=[O:11])([O-:3])=[O:2].Cl.[CH2:15]([O:22][NH2:23])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>N1C=CC=CC=1>[CH2:15]([O:22][NH:23][S:10]([C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2])(=[O:12])=[O:11])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
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참가 물질

4

반응물 2

HCID 155402-Nitrobenzenesulfonyl chlorideHCID 102312Benzyloxyamine hydrochloride

생성물 1

HCID 9839578N-(Benzyloxy)-2-nitrobenzenesulfonamide수율 69.6%

시약·촉매·용매 1

HCID 1049Pyridine용매2회

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온도
20 °C

실험 절차

A solution of 2-nitrobenzene-1-sulfonyl chloride (500 g, 2.26 mol) in pyridine (1500 mL) was added dropwise to a solution of O-benzylhydroxylamine hydrochloride (400 g, 2.51 mol) in pyridine (1500 mL) at 0° C. The reaction mixture was then stirred at 20° C. overnight. The mixture was concentrated in vacuum, diluted with DCM and washed with HCl (10%) three times. The combined organic layer was concentrated in vacuum and re-crystallized with DCM to afford N-(benzyloxy)-2-nitrobenzenesulfonamide (485 g, 62.6%) as a yellow solid.

후처리

  1. concentrationThe mixture was concentrated in vacuum
  2. additiondiluted with DCM
  3. washwashed with HCl (10%) three times
  4. concentrationThe combined organic layer was concentrated in vacuum
  5. customre-crystallized with DCM

출처 및 근거

ORD 기록
ord-113df1ba909d48479100928e2d5509ea
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108966B2

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