m-Xylyl bromide → N-benzyl-2-(3-methylbenzyl)-morpholin-3-one
Reaction equation
C(N1CCO[C@H]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([CH2:21]O)[CH:16]=2)C1)(OC(C)(C)C)=O.[CH2:23]([N:30]1[CH2:35][CH2:34][O:33][CH2:32][C:31]1=[O:36])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.CC1C=C(C=CC=1)CBr>>[CH2:23]([N:30]1[CH2:35][CH2:34][O:33][CH:32]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([CH3:21])[CH:16]=2)[C:31]1=[O:36])[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1Participants
4
Procedure
N-Benzyl-2-(3-methylbenzyl)-morpholin-3-one was prepared as described for example 70, intermediate (b), but using 4-benzylmorpholine-3-one and 3-methylbenzyl bromide and was isolated as a pale yellow oil.
Workup
- customwas isolated as a pale yellow oil
Sources & evidence
- ORD record
- ord-45d94fe4050648f9865ac0902907f25f
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07323466B2
Reaction notes
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