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Borane → N-benzyl-2-(2-difluoromethoxy-benzyl)-morpholine

HRID 2253023
Notes
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Reaction equation

HRID 2253023 reaction equation
C(N1CCO[C@H](CC2C=CC=C(C=CC3C=NC=CC=3)C=2)C1)(OC(C)(C)C)=O.[CH2:29]([N:36]1[CH2:41][CH2:40][O:39][CH:38]([CH2:42][C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][C:44]=2[O:49][CH:50]([F:52])[F:51])[C:37]1=O)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1.B>>[CH2:29]([N:36]1[CH2:41][CH2:40][O:39][CH:38]([CH2:42][C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][C:44]=2[O:49][CH:50]([F:51])[F:52])[CH2:37]1)[C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 6331BoraneHCID 67073097N-benzyl-2-(2-difluoromethoxy-benzyl)-morpholin-3-oneHCID 67073511N-Boc-(R)-2-(3-(2-(3-pyridinyl)vinyl)-benzyl)morpholine

Product 1

HCID 67073057N-benzyl-2-(2-difluoromethoxy-benzyl)-morpholine

Procedure

N-Benzyl-2-(2-difluoromethoxy-benzyl)-morpholine was prepared as described for example 70, intermediate (a), but using N-benzyl-2-(2-difluoromethoxy-benzyl)-morpholin-3-one and borane and was isolated as a pale yellow oil.

Workup

  • customwas isolated as a pale yellow oil
  • Sources & evidence

    ORD record
    ord-375723f8d3cd4f86889e5973d5020021
    Source dataset
    uspto-grants-2008_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07323466B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes