Aniline → Benzenesulfonamide, 4-methyl-N-phenyl-

HRID 2395925

反応式

HRID 2395925 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[C:15]1([CH3:25])[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][CH:16]=1.C(OCC)(=O)C.CCCCCC>C(Cl)Cl.CCOCC>[C:2]1([NH:1][S:21]([C:18]2[CH:19]=[CH:20][C:15]([CH3:25])=[CH:16][CH:17]=2)(=[O:23])=[O:22])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

7

実験手順

Aniline (1.86 g, 0.02 mol) was dissolved in methylene chloride under nitrogen and triethylamine (3.8 mL, 0.02 mol) was added. This solution wascooled in an ice bath and a solution of p-toluenesulfonyl chloride (3.8 g, 0.02 mol) was added dropwise via a syringe. After stirring this solution for 4 h at room temperature, TLC analysis (silica gel, 20% ethyl acetate/hexane) indicated completion of the reaction. The reaction mixturewas poured into ether and the precipitate filtered. The ether layer was washed with water, dried over MgSO4 and concentrated to yield an oilymaterial. This crude product was chromatographed on silica using 35% ethyl acetate and hexane to obtain a solid which was further recrystallized in methylene chloride/hexane; m.p. 104° C.; 1H NMR (CDCl3) δ2.36 (s, 3H), 7.07-7.25 (m, 8H), 7.67-7.69 (d, 2H).

後処理

  1. customThis solution wascooled in an ice bath
  2. customcompletion of the reaction
  3. filtrationthe precipitate filtered
  4. washThe ether layer was washed with water
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated
  7. customto yield an oilymaterial
  8. customThis crude product was chromatographed on silica using 35% ethyl acetate and hexane
  9. customto obtain a solid which
  10. customwas further recrystallized in methylene chloride/hexane

出典と根拠

ORDレコード
ord-c252f627c2fd4c92ac36b2911bd08852
出典データセット
uspto-grants-1996_02
特許番号
US05491072

関連ノート

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