Potassium Iodide → 4-(p-bromophenyl)-4-hydroxy-N,N-dimethyl-alpha,alpha-diphenylpiperidine-1-butyramide hydrate

HRID 482377ノート

反応式

HRID 482377 の反応式
[Br-].[CH3:2][N+:3]([CH3:21])=[C:4]1[C:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH2:7][CH2:6][O:5]1.Cl.[Br:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]2([OH:36])[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]2)=[CH:26][CH:25]=1.C(=O)([O-])[O-].[Na+].[Na+].[I-].[K+]>O.CC(C)CC(=O)C>[OH2:5].[Br:23][C:24]1[CH:29]=[CH:28][C:27]([C:30]2([OH:36])[CH2:31][CH2:32][N:33]([CH2:6][CH2:7][C:8]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[C:4]([N:3]([CH3:21])[CH3:2])=[O:5])[CH2:34][CH2:35]2)=[CH:26][CH:25]=1

参加物

7

実験手順

A mixture of 12.1 parts of dimethyl (tetrahydro-3,3-diphenyl-2-furylidene) ammonium bromide, 8.8 parts of 4-(p-bromophenyl)-4-piperidinol hydrochloride, 10.6 parts of sodium carbonate, 0.5 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 14 hours with water separator. The reaction mixture is cooled and water (200 parts) is added. The organic layer is separated, washed with diluted sodium hydroxide solution, dried, filtered, and while stirring the filtrate, the product is crystallized. It is filtered off and recrystallized from 80 parts of 4-methyl-2-pentanone (activated charcoal), yielding 4-(p-bromophenyl)-4-hydroxy-N,N-dimethyl-α,α-diphenylpiperidine-1-butyramide hydrate; m.p. 123.7° C.

後処理

  1. temperatureThe reaction mixture is cooled
  2. customThe organic layer is separated
  3. washwashed with diluted sodium hydroxide solution
  4. customdried
  5. filtrationfiltered
  6. stirringwhile stirring the filtrate
  7. customthe product is crystallized
  8. filtrationIt is filtered off
  9. customrecrystallized from 80 parts of 4-methyl-2-pentanone (activated charcoal)

出典と根拠

ORDレコード
ord-49d8828a0da143bd8ce8f5b9afa09162
出典データセット
uspto-grants-1998_08
特許番号
US05798093

反応ノート

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