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Peracetic Acid → N-methyl-N-(2,3-dichlorophenyl)-2-pyridinesulfonamide 1-oxide

HRID 3749
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HRID 3749 반응식
[CH3:1][N:2]([C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[C:13]=1[Cl:19])[S:3]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][N:7]=1)(=[O:5])=[O:4].C(OO)(=[O:22])C>>[CH3:1][N:2]([C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[C:13]=1[Cl:19])[S:3]([C:6]1[N+:7]([O-:22])=[CH:8][CH:9]=[CH:10][CH:11]=1)(=[O:4])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6585Peracetic AcidHCID 14097678N-methyl-N-(2,3-dichlorophenyl)-2-pyridinesulfonamide

생성물 1

HCID 14097679N-methyl-N-(2,3-dichlorophenyl)-2-pyridinesulfonamide 1-oxide

실험 절차

N-methyl-N-(2,3-dichlorophenyl)-2-pyridinesulfonamide (1.7 g, 5.3 mmol) is treated with 40% peracetic acid (approx. 12 ml) at 35°-45° under N2 for 14 hours. The excess peracetic acid is removed under vacuum, and the residue is diluted with methylene chloride, poured into water, neutralized with aq. sodium bicarbonate, washed with brine, dried and evaporated to dryness to give, after purification, the title compound (compound 1, Table A).

후처리

  1. customThe excess peracetic acid is removed under vacuum
  2. additionthe residue is diluted with methylene chloride
  3. additionpoured into water
  4. washwashed with brine
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customdried
  • customevaporated to dryness
  • customto give
  • customafter purification
  • 출처 및 근거

    ORD 기록
    ord-97bc304407514ba8bc93cfbe5770416a
    출처 데이터셋
    uspto-grants-1988_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04722749

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