Hydrochloric Acid → Sulfabenz

HRID 889511

反応式

HRID 889511 の反応式
Cl.[C:2]1([NH:8][S:9]([C:12]2[CH:17]=[CH:16][C:15]([NH:18]C(=O)C)=[CH:14][CH:13]=2)(=[O:11])=[O:10])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(O)C>[NH2:18][C:15]1[CH:16]=[CH:17][C:12]([S:9]([NH:8][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)(=[O:11])=[O:10])=[CH:13][CH:14]=1

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 7700104-Acetamidobenzenesulfonanilide

生成物 1

HCID 31390Sulfabenz

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

An aqueous 6N solution of HCl (40 mL) was cautiously added with stirring to a solution of 3 (20 g, 68 mmol) in ethanol (80 mL). After heating under reflux for 3 h, the reaction mixture was evaporated to dryness in vacuo and the residue was dissolved in water. The pH of the solution was adjusted to 8-9 using 1N aq. NH4OH. After stirring for 1 h, the white solid that gradually precipitated was collected by filtration. The filter cake was washed with ice-cold water, dried under vacuum, and recrystallized from hot ethanol to give to give 4-amino-N-phenyl-benzenesulfonamide (4) (also called 207-33 or LED207) (10.9 g, 65%) as a white solid, mp 194-195° C. 1H NMR (CD3COCD3, 300 MHz) δ 8.64 (br s, 1H), 7.50-7.45 (m, 2H), 7.25-7.18 (m, 4H), 7.04-6.98 (m, 1H), 6.67-6.62 (m, 2H), 5.44 (br s, 2H); 13C NMR (CD3COCD3, 75 MHz) δ 152.9, 138.8, 129.3 (2C), 129.1 (2C), 126.3, 124.0, 120.5 (2C), 113.1 (2C).

後処理

  1. temperatureAfter heating
  2. temperatureunder reflux for 3 h
  3. customthe reaction mixture was evaporated to dryness in vacuo
  4. dissolutionthe residue was dissolved in water
  5. customthe white solid that gradually precipitated
  6. filtrationwas collected by filtration
  7. washThe filter cake was washed with ice-cold water
  8. customdried under vacuum
  9. customrecrystallized from hot ethanol
  10. customto give

出典と根拠

ORDレコード
ord-d60d9bed05b141f19636cc80923fbc7b
出典データセット
uspto-grants-2012_08
特許番号
US08252841B2

関連ノート

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