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Hydrochloric Acid → Venlafaxine Hydrochloride

HRID 20621
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인쇄 미리보기

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HRID 20621 반응식
[CH3:1][N:2]([CH2:4][CH:5]([C:14]1([OH:20])[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)[C:6]1[CH:7]=[CH:8][C:9]([O:12][CH3:13])=[CH:10][CH:11]=1)[CH3:3].C(OC(C)C)(=O)C.[ClH:28]>>[CH3:1][N:2]([CH2:4][CH:5]([C:14]1([OH:20])[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]1)[C:6]1[CH:7]=[CH:8][C:9]([O:12][CH3:13])=[CH:10][CH:11]=1)[CH3:3].[ClH:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 5656VenlafaxineHCID 7915Isopropyl Acetate

생성물 1

HCID 62923Venlafaxine Hydrochloride수율 88%

실험 절차

To the solution of venlafaxine base in isopropyl acetate from example 1 (66 ml, 10 mmol) 5 ml of 2 M aqueous HCl were added. The mixture was heated and water was removed by azeotropic distillation using a Dean-Starck trap. When all water was removed from the mixture, the product began slowly to crystallize. The obtained suspension was heated under reflux temperature for 1.5 h, then cooled and filtered. 2.75 g (88% from N,N-didesmethyl venlafaxine hydrochloride) of pure venlafaxine hydrochloride form I (HPLC: 99.65 area %) were obtained.

후처리

  1. temperature
The mixture was heated
  • customwater was removed by azeotropic distillation
  • customWhen all water was removed from the mixture
  • customto crystallize
  • temperatureThe obtained suspension was heated
  • temperatureunder reflux temperature for 1.5 h
  • temperaturecooled
  • filtrationfiltered
  • 출처 및 근거

    ORD 기록
    ord-b19b7219e7da48a7bfb6ddb406b91cc9
    출처 데이터셋
    uspto-grants-2010_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07745664B2

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