Hydroxyamine hydrochloride → 1-Acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine oxime

HRID 370886노트

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HRID 370886 반응식
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10](=O)[C:11]2[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:12]=2[OH:19])[CH2:6][CH2:5]1)(=[O:3])[CH3:2].Cl.[NH2:22][OH:23].C([O-])(=O)C.[NH4+]>O>[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10](=[N:22][OH:23])[C:11]2[CH:16]=[C:15]([O:17][CH3:18])[CH:14]=[CH:13][C:12]=2[OH:19])[CH2:6][CH2:5]1)(=[O:3])[CH3:2]

참가 물질

5

실험 절차

A solution of 15.5 g of 1-acetyl-4-(2-hydroxy-5-methoxybenzoyl)piperidine, 7.0 g of hydroxylamine hydrochloride, 9.5 g of ammonium acetate and 75 ml of water was heated under reflux for 20 hrs. The solution was poured into water and extracted with dichloromethane. The dichloromethane extract was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to give an oil. The oil was triturated with hot toluene. The toluene was decanted and the oil was triturated with ether to give a solid. The tolulene triturant, upon standing, yielded a solid. The solids were combined and recrystallized from acetonitrile to yield 2.8 g (17.4%) of product, mp, 191°-193°, as a mixture of E- and Z-isomers. The chromatogram showed 2 spots.

후처리

  1. temperatureunder reflux for 20 hrs
  2. extractionextracted with dichloromethane
  3. extractionThe dichloromethane extract
  4. washwas washed with water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was removed in vacuo
  7. customto give an oil
  8. customThe oil was triturated with hot toluene
  9. customThe toluene was decanted
  10. customthe oil was triturated with ether
  11. customto give a solid
  12. customyielded a solid
  13. customrecrystallized from acetonitrile

출처 및 근거

ORD 기록
ord-1b85797003b1489cb3dabf1d4a71a1a3
출처 데이터셋
uspto-grants-1985_07
특허 번호
US04528376

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