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Hydroxyamine hydrochloride → 2,6-Dimethyl-1-(phenylmethyl)-4-piperidinone oxime

HRID 1492730
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인쇄 미리보기

반응식

HRID 1492730 반응식
[CH2:1]([N:8]1[CH:13]([CH3:14])[CH2:12][C:11](=O)[CH2:10][CH:9]1[CH3:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[NH2:18][OH:19].C([O-])(=O)C.[Na+]>CO.O>[CH2:1]([N:8]1[CH:13]([CH3:14])[CH2:12][C:11](=[N:18][OH:19])[CH2:10][CH:9]1[CH3:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 15714117(2S,6S)-1-benzyl-2,6-dimethylpiperidin-4-one

생성물 1

HCID 157141182,6-Dimethyl-1-(phenylmethyl)-4-piperidinone oxime수율 48.6%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water
용매

반응 조건

온도
60 °C

실험 절차

10 g of 1-benzyl-2,6-dimethyl-4-piperidone (prepared from benzylamine and ethyl crotonate in analogy to Bull. Chem. Soc. Japan 31 (1958) 418) are dissolved in 60 ml of methanol and this solution is added dropwise to a solution of 3.8 g of hydroxylamine hydrochloride and 4.5 g of sodium acetate in 150 ml of water. The mixture is stirred at 60° C. for 2 h and cooled to 0° C., and the oxime which has separated out is filtered off with suction. Drying results in 5.2 g of the title compound.

후처리

  1. temperaturecooled to 0° C.
  2. customthe oxime which has separated out
  3. filtrationis filtered off with suction
  4. customDrying

출처 및 근거

ORD 기록
ord-990a33963fb14dfa80cee02850273089
출처 데이터셋
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05374731

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