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4-(4-Pyrrolidin-1-ylcarbonylbenzyl)-nitrobenzene → 4-[4-(1-Pyrrolidinecarbonyl)benzyl]-phenylamine

HRID 634823
Notes
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Reaction equation

HRID 634823 reaction equation
[N:1]1([C:6]([C:8]2[CH:23]=[CH:22][C:11]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=3)=[CH:10][CH:9]=2)=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1>[Pd].C(O)C>[N:1]1([C:6]([C:8]2[CH:23]=[CH:22][C:11]([CH2:12][C:13]3[CH:18]=[CH:17][C:16]([NH2:19])=[CH:15][CH:14]=3)=[CH:10][CH:9]=2)=[O:7])[CH2:2][CH2:3][CH2:4][CH2:5]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 120943914-(4-Pyrrolidin-1-ylcarbonylbenzyl)-nitrobenzene

Product 1

HCID 120943904-[4-(1-Pyrrolidinecarbonyl)benzyl]-phenylamineYield 102.5%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

A mixture of 4-(4-pyrrolidin-1-ylcarbonylbenzyl)-nitrobenzene (202 mg, 065 mmol), 10% palladium on carbon (110 mg), and ethanol (20 mL) was hydrogenated at 40 psi for 16 hours. The mixture was filtered through a Celite pad, and solvents evaporated to give 4-[4-(1-pyrrolidinecarbonyl)benzyl]-phenylamine as a white solid (187 mg, 99%).

Workup

  1. filtrationThe mixture was filtered through a Celite pad, and solvents
  2. customevaporated

Sources & evidence

ORD record
ord-c05981ef598140a0a02cf711fd8064de
Source dataset
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06184242B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes