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3-(R)-(1-BOC-2-(S)-pyrrolidinyl)-4-nitrobutanol → 3-(R)-(1-BOC-pyrrolidin-2-(S)-yl)pyrrolidine

HRID 1450102
Notes
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Reaction equation

HRID 1450102 reaction equation
[C:1]([N:8]1[CH2:12][CH2:11][CH2:10][C@H:9]1[C@@H:13]([CH2:17][N+:18]([O-])=O)[CH2:14][CH2:15]O)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2]>CO.[Pd]>[C:1]([N:8]1[CH2:12][CH2:11][CH2:10][C@H:9]1[C@@H:13]1[CH2:14][CH2:15][NH:18][CH2:17]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 228695313-(R)-(1-BOC-2-(S)-pyrrolidinyl)-4-nitrobutanol

Product 1

HCID 228695333-(R)-(1-BOC-pyrrolidin-2-(S)-yl)pyrrolidine

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

The ether compound from step 471a was treated by hydrogenation at 4 atm H2 over Pd/C in methanol to give the tile compound.

Workup

  1. customto give the tile compound

Sources & evidence

ORD record
ord-0c8c306ab2af42f19a89b9d2eeb5fa2f
Source dataset
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05599816

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes