Hydrochloric Acid → {3-[(Methanesulfonyl)amino]phenyl}acetic acid

HRID 227451

반응식

HRID 227451 반응식
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[NH2:6][C:7]1[CH:8]=[C:9]([CH2:13][C:14]([OH:16])=[O:15])[CH:10]=[CH:11][CH:12]=1.C(=O)([O-])[O-].[Na+].[Na+].Cl>O>[CH3:1][S:2]([NH:6][C:7]1[CH:8]=[C:9]([CH2:13][C:14]([OH:16])=[O:15])[CH:10]=[CH:11][CH:12]=1)(=[O:4])=[O:3]

참가 물질

6

반응 조건

온도
85 °C

실험 절차

Methanesulphonylchloride (1.70 ml) was added to a stirred mixture of 3-aminophenylacetic acid (3.2 g) and sodium carbonate (5.44 g) in water (36 ml), and the mixture was heated at 85° C. with stirring for 4 h, allowed to cool and acidified with conc. hydrochloric acid to pH 2. After leaving to stand at approximately 4° C. for 18 h, a solid was filtered off, and the residue washed with water and ether. The aqueous and ether filtrates were combined and evaporated in vacuo to give a solid, which was dissolved in hot water, the solution was filtered whilst still hot and the filtrate left to cool before standing at 4° C. for 18 h. The precipitated solid was filtered, washed with a small quantity of cold water and dried in vacuo to give the title compound as a pale yellow solid (0.417 g).

후처리

  1. temperatureto cool
  2. customAfter leaving
  3. waitto stand at approximately 4° C. for 18 h
  4. filtrationa solid was filtered off
  5. washthe residue washed with water and ether
  6. customevaporated in vacuo
  7. customto give a solid, which
  8. filtrationthe solution was filtered whilst still hot and the filtrate
  9. waitleft
  10. temperatureto cool
  11. waitbefore standing at 4° C. for 18 h
  12. filtrationThe precipitated solid was filtered
  13. washwashed with a small quantity of cold water
  14. customdried in vacuo

출처 및 근거

ORD 기록
ord-405696ea706a4427860574e3b2cbb7e8
출처 데이터셋
uspto-grants-2009_07
특허 번호
US07560548B2

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