Butanal → 1-Butyl-4-(4-methoxyphenyl)piperazine dihydrochloride

HRID 1156287

반응식

HRID 1156287 반응식
[ClH:1].Cl.[CH3:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]2)=[CH:7][CH:6]=1.[CH:17](=O)[CH2:18][CH2:19][CH3:20].C([O-])(=O)C.[Na+].[H][H]>[Pd].CO>[ClH:1].[ClH:1].[CH2:17]([N:14]1[CH2:15][CH2:16][N:11]([C:8]2[CH:7]=[CH:6][C:5]([O:4][CH3:3])=[CH:10][CH:9]=2)[CH2:12][CH2:13]1)[CH2:18][CH2:19][CH3:20]

참가 물질

7

실험 절차

A mixture of 13.2 parts of 1-(4-methoxyphenyl)piperazine dihydrochloride, 5.1 parts of 1-butanal, 9 parts of sodium acetate and 80 parts of methanol is hydrogenated at normal pressure and at room temperature with 1 part of palladium-on-charcoal catalyst. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. Water is added to the residue and the product is precipitated. It is filtered off, washed with water and converted into the hydrochloride salt in ethanol and 2-propanol. Upon the addition of 2,2'-oxybispropane, the salt is precipitated. It is filtered off and crystallized from a mixture of ethanol and 2,2'-oxybispropane, yielding 13.1 parts (81%) of 1-butyl-4-(4-methoxyphenyl)piperazine dihydrochloride; mp. 214.2° C.

후처리

  1. filtrationthe catalyst is filtered off
  2. customthe filtrate is evaporated
  3. additionWater is added to the residue
  4. customthe product is precipitated
  5. filtrationIt is filtered off
  6. washwashed with water
  7. additionUpon the addition of 2,2'-oxybispropane
  8. customthe salt is precipitated
  9. filtrationIt is filtered off
  10. customcrystallized from a mixture of ethanol and 2,2'-oxybispropane

출처 및 근거

ORD 기록
ord-b206d30cabf54b479e251fd609922b08
출처 데이터셋
uspto-grants-1982_06
특허 번호
US04335125

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