Potassium Iodide → 1-(2-Phenylethyl)piperidinyl-methanone hydrochloride

HRID 1493194ノート

反応式

HRID 1493194 の反応式
[ClH:1].C=O.CC(C1C=CC(C([CH:15]2[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]2)=O)=CC=1)C.Br[CH2:22][CH2:23][C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.[C:30]([O-])([O-])=[O:31].[K+].[K+].[I-].[K+]>C1(C)C=CC=CC=1>[ClH:1].[C:24]1([CH2:23][CH2:22][N:18]2[CH2:17][CH2:16][CH2:15][CH2:20][CH:19]2[CH:30]=[O:31])[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1

参加物

7

反応物 5

HCID 4875Potassium IodideHCID 7666Phenethyl bromideHCID 11430Potassium CarbonateHCID 19933572Methanone hydrochlorideHCID 222382884-[4-(Propan-2-yl)benzoyl]piperidine

生成物 1

HCID 867448161-(2-Phenylethyl)piperidinyl-methanone hydrochloride

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

[4-(1-methylethyl)phenyl]1-(2-phenylethyl)-piperidinyl]-methanone HCl. A solution of [4-(1-methylethyl)phenyl](4-piperidinyl)-methanone (43 g, 0.19 mol) in toluene (500 ml) was treated with 2-bromoethylbenzene (37 g, 0.2 mol), K2CO3 (25 g, 0.18 mol), KHCO3 (25 g, 0.25 mol) and potassium iodide (0.1 g) and the mixture heated on a steam bath for 68 h. The reaction mixture was filtered and the filtrate treated with ethereal hydrogen chloride until acid to congo red indicator paper. The resultant precipitate was filtered off and recrystallized twice from CH3OH/butanone to give [4-(1-methylethyl)-phenyl][1-(2-phenylethyl)piperidinyl-methanone hydrochloride, mp 251°-253° C. By following the sodium borohydride reduction procedure of the foregoing example there is obtained the desired product of this example.

後処理

  1. temperaturethe mixture heated on a steam bath for 68 h
  2. filtrationThe reaction mixture was filtered
  3. additionthe filtrate treated with ethereal hydrogen chloride until acid to congo red indicator paper
  4. filtrationThe resultant precipitate was filtered off
  5. customrecrystallized twice from CH3OH/butanone

出典と根拠

ORDレコード
ord-9c04e6c0bfa94dab84e911d742e1aa08
出典データセット
uspto-grants-1991_06
特許番号
US05021428

反応ノート

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