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Hydroxyamine hydrochloride → Ethyl 4-(hydroxyimino)-5-oxo-1-phenyl-3-pyrrolidineacetate

HRID 1590262
Notes
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Reaction equation

HRID 1590262 reaction equation
O=[C:2]1[C:6](=[O:7])[N:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:4][CH:3]1[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16].Cl.[NH2:21][OH:22]>N1C=CC=CC=1>[OH:22][N:21]=[C:2]1[C:6](=[O:7])[N:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:4][CH:3]1[CH2:14][C:15]([O:17][CH2:18][CH3:19])=[O:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 443297Hydroxyamine hydrochlorideHCID 57059855Ethyl 4,5-dioxo-1-phenyl-3-pyrrolidineacetate

Product 1

HCID 86746704Ethyl 4-(hydroxyimino)-5-oxo-1-phenyl-3-pyrrolidineacetate

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

A solution of product of Example 62 in pyridine is treated with an excess of hydroxylamine hydrochloride and the reaction is stirred at room temperature for 2 d. The solution is concentrated in vacuo and the residue is chromatographed on silica gel to give the title compound.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  1. concentrationThe solution is concentrated in vacuo
  2. customthe residue is chromatographed on silica gel

Sources & evidence

ORD record
ord-94d20b50deb44793a86bc515156acfef
Source dataset
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05202344

Reaction notes

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