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Methanol → HCID 14404104, 화합물

HRID 465501
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HRID 465501 반응식
S(Cl)(Cl)=O.[C:5]([C:8]1[CH:13]=[CH:12][C:11]([S:14]([CH2:17][N+:18]([O-:20])=[O:19])(=[O:16])=[O:15])=[CH:10][CH:9]=1)([OH:7])=[O:6].[CH3:21]O>>[CH3:21][O:6][C:5]([C:8]1[CH:9]=[CH:10][C:11]([S:14]([CH2:17][N+:18]([O-:20])=[O:19])(=[O:15])=[O:16])=[CH:12][CH:13]=1)=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 14404103HCID 14404103, 화합물

생성물 1

HCID 14404104HCID 14404104, 화합물

실험 절차

Thionyl chloride (0.33 ml, 4.5 mmol) was added dropwise to a stirred solution of (4-carboxyphenylsulphonyl)nitromethane (1.0 g, 4 mmol) in methanol (12 ml) cooled in an ice-salt bath. The mixture was stirred for 16 hours at ambient temperature and the solvent evaporated. The residue was purified by MPLC eluting with dichloromethane, gradually increasing to methanol/dichloromethane (1:50 v/v), to give (4-methoxycarbonylphenylsulphonyl)nitromethane (0.45 g), m.p. 106°-108° C.; microanalysis, found: C, 41.8; H, 3.5; N, 5.2%; C9H9NO6S requires: C, 41.7; H, 3.5: N, 5.4%.

후처리

  1. temperaturecooled in an ice-salt bath
  • customthe solvent evaporated
  • customThe residue was purified by MPLC
  • washeluting with dichloromethane
  • temperaturegradually increasing to methanol/dichloromethane (1:50 v/v)
  • 출처 및 근거

    ORD 기록
    ord-ca3ca7678fc044288dd39f3ae20d2b5a
    출처 데이터셋
    uspto-grants-1992_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05153227

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