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Methanol → Methyl 2-[(3-hydroxypropyl)sulfonyl]-5-sulfamoylbenzoate

HRID 2118580
ノート
印刷プレビュー

反応式

HRID 2118580 の反応式
[OH:1][CH2:2][CH2:3][CH2:4][S:5][C:6]1[CH:11]=[CH:10][C:9]([S:12]([NH2:15])(=[O:14])=[O:13])=[CH:8][C:7]=1[C:16]([OH:18])=[O:17].OS(O)(=O)=O.[CH3:24]O>>[OH:1][CH2:2][CH2:3][CH2:4][S:5][C:6]1[CH:11]=[CH:10][C:9]([S:12]([NH2:15])(=[O:14])=[O:13])=[CH:8][C:7]=1[C:16]([O:18][CH3:24])=[O:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 13960351HCID 13960351、化合物

生成物 1

HCID 13960352Methyl 2-[(3-hydroxypropyl)sulfonyl]-5-sulfamoylbenzoate

実験手順

4-(3-hydroxypropylthio)-3-carboxybenzene-sulfonamide (15 g, 0.0515 mol) and concentrated H2SO4 (4 ml) were dissolved in methanol (150 ml) and refluxed on a steam bath for about 5 hours. The solvent was removed and the residue was treated with water. The mixture was extracted with ethylacetate, which was washed with water, saturated sodium bicarbonate, water and brine. After drying, removal of the solvent left a tannish solid. Recrystallization from 1,2-dichloroethane gave 13.5 g of a white solid. M.p.=123°-125°.

後処理

  1. temperaturerefluxed on a steam bath for about 5 hours
  • customThe solvent was removed
  • additionthe residue was treated with water
  • extractionThe mixture was extracted with ethylacetate, which
  • washwas washed with water, saturated sodium bicarbonate, water and brine
  • customAfter drying
  • customremoval of the solvent
  • waitleft a tannish solid
  • customRecrystallization from 1,2-dichloroethane
  • 出典と根拠

    ORDレコード
    ord-6f0fe8d684c841c9b62bd4e57bf96653
    出典データセット
    uspto-grants-1987_07
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US04678855

    反応ノート

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