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Ammonia → N,N-Didesmethylvenlafaxine

HRID 229946
ノート
印刷プレビュー

反応式

HRID 229946 の反応式
CO.N.[C:4]([CH:6]([C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=1)[C:7]1([OH:13])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1)#[N:5]>[Ni].C(O)(=O)C>[NH2:5][CH2:4][CH:6]([C:7]1([OH:13])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1)[C:14]1[CH:15]=[CH:16][C:17]([O:20][CH3:21])=[CH:18][CH:19]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 222AmmoniaHCID 887Methanol2 回HCID 9899621(1-Hydroxycyclohexyl)(4-methoxyphenyl)acetonitrile

生成物 1

HCID 9795857N,N-Didesmethylvenlafaxine収率 70%

試薬・触媒・溶媒 2

HCID 935Nickel触媒HCID 176Acetic Acid溶媒2 回

実験手順

The reactor was charged with 25.0 g of Raney-Ni (Kawaken, Grace 2400, 2724, Degussa B111W, 112W), and 250 ml of MeOH and 25 ml of an ammonia solution (25% NH3) were added. To the mixture was added 50g of 1-[cyano(4-methoxyphenyl)methyl]cyclohexanol, followed by 250 ml of MeOH. The reactor was settled and purged with N2 gas two or three times. After fully purged with N2, the reactor was purged with H2 gas two or three times. Internal pressure of the reactor was adjusted to 60 psi and the reaction mixture was stirred. After 20 to 30 hours of reaction at room temperature (about 10 to 20° C.), in-process analysis of a sample of mixture was made. After the reaction was completed, Ra—Ni was removed by filtration with a celite pad. The filtrate was distilled under reduced pressure until all of the solvent was evaporated, and 200 ml of isopropyl alcohol and 400 ml of ethyl acetate were added to the residue oil to dissolve the resulting product to give a clear or a little hazy solution. To the solution was added 10 ml of acetic acid dropwise, and an exothermic reaction began with some fumes given off. After about 10 to 20 minutes of adding all of the acetic acid, a solid began to form. The solution was stirred for about one hour, filtered and washed with ethyl acetate to give the desired product, 1-[2-amino-1-(4-methoxyphenyl)ethyl]-cyclohexanol, 44.2 g (yield 70%, purity 99%).

後処理

  1. additionwere added
  2. custompurged with N2 gas two or three times
  3. customAfter fully purged with N2
  4. customthe reactor was purged with H2 gas two or three times
  5. customAfter 20 to 30 hours of reaction at room temperature (about 10 to 20° C.)
  6. customRa—Ni was removed by filtration with a celite pad
  7. distillationThe filtrate was distilled under reduced pressure until all of the solvent
  8. customwas evaporated
  9. addition200 ml of isopropyl alcohol and 400 ml of ethyl acetate were added to the residue oil
  10. dissolutionto dissolve the resulting product
  11. customto give a clear or a little hazy solution
  12. customan exothermic reaction
  13. customto form
  14. stirringThe solution was stirred for about one hour
  15. filtrationfiltered
  16. washwashed with ethyl acetate

出典と根拠

ORDレコード
ord-f3a8d5ba53d3497db9f217a7d277c250
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07563931B2

反応ノート

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