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4-Bromobenzaldehyde → Benzyl 4-[(4-bromophenyl)methyl]piperazine-1-carboxylate

HRID 43350
Notes
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Reaction equation

HRID 43350 reaction equation
N1(C(OCC2C=CC=CC=2)=O)CCNCC1.BrC1C=CC(C=O)=CC=1.[Br:26][C:27]1[CH:32]=[CH:31][C:30]([CH2:33][N:34]2[CH2:39][CH2:38][N:37]([C:40]([O:42][CH2:43][C:44]3[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=3)=[O:41])[C@@H:36](C)[CH2:35]2)=[CH:29][CH:28]=1>>[Br:26][C:27]1[CH:28]=[CH:29][C:30]([CH2:33][N:34]2[CH2:35][CH2:36][N:37]([C:40]([O:42][CH2:43][C:44]3[CH:45]=[CH:46][CH:47]=[CH:48][CH:49]=3)=[O:41])[CH2:38][CH2:39]2)=[CH:31][CH:32]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 707414-BromobenzaldehydeHCID 643495Benzyl piperazine-1-carboxylateHCID 25224210Phenylmethyl (2S)-4-[(4-bromophenyl)methyl]-2-methyl-1-piperazine Carboxylate

Product 1

HCID 67128009Benzyl 4-[(4-bromophenyl)methyl]piperazine-1-carboxylate

Procedure

The title compound was prepared from phenylmethyl 1-piperazinecarboxylate and 4-bromobenzaldehyde using a method to that described for D6

Sources & evidence

ORD record
ord-2dc8ccd60ede4c1297b0d65fbfc72a74
Source dataset
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08536182B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes