2-Phenylbutyric Acid → 4'-(1-Oxo-2-phenylbutyl)methanesulfonanilide

HRID 1414266

反応式

HRID 1414266 の反応式
[CH3:1][S:2]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)(=[O:4])=[O:3].[C:12]1([CH:18]([CH2:22][CH3:23])[C:19](O)=[O:20])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>O>[O:20]=[C:19]([C:9]1[CH:8]=[CH:7][C:6]([NH:5][S:2]([CH3:1])(=[O:4])=[O:3])=[CH:11][CH:10]=1)[CH:18]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:22][CH3:23]

参加物

4

反応物 2

HCID 70122-Phenylbutyric AcidHCID 70970Methanesulfonamide, N-phenyl-

生成物 1

HCID 214866524'-(1-Oxo-2-phenylbutyl)methanesulfonanilide収率 23%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Methanesulfonanilide (40 g., 0.234 mole) is added over a 10 minute period with stirring to polyphosphoric acid (400 g.) heated to 90°-100°C. Heating and stirring are continued for additional 10 minutes, at which time 2-phenylbutanoic acid (36.0 g., 0.219 mole) is added portionwise during 20 minutes. After heating and stirring for 10 minutes, the solution is poured into water (600 ml.) and ice (400 g.) with stirring. The water is decanted and ethyl ether (200 ml.) is added to the remaining oil with stirring. After cooling in ice water, the product crystallizes and is collected: 18.4 g., m.p. 143°-147°C. Recrystallization from isopropanol yields 15.7 g. (23% yield), m.p. 148°-150°C.

後処理

  1. temperatureheated to 90°-100°C
  2. temperatureHeating
  3. additionis added portionwise during 20 minutes
  4. temperatureAfter heating
  5. stirringstirring for 10 minutes
  6. stirringwith stirring
  7. customThe water is decanted
  8. additionethyl ether (200 ml.) is added to the remaining oil
  9. stirringwith stirring
  10. temperatureAfter cooling in ice water
  11. customthe product crystallizes
  12. customis collected
  13. customRecrystallization from isopropanol
  14. customyields 15.7 g

出典と根拠

ORDレコード
ord-58cc82de06ba4bb5a678ac389eed67c7
出典データセット
uspto-grants-1977_01
特許番号
US04001229

関連ノート

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