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

HRID 1493194노트

반응식

HRID 1493194 반응식
[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

참가 물질

7

반응물 5

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

생성물 1

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

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

[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.

후처리

  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

출처 및 근거

ORD 기록
ord-9c04e6c0bfa94dab84e911d742e1aa08
출처 데이터셋
uspto-grants-1991_06
특허 번호
US05021428

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