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Dimethyl Sulfoxide → 1-(p-nitrobenzyloxycarbonyl)-4-oxo-L-proline p-methoxybenzyl ester

HRID 893169
Notes
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Reaction equation

HRID 893169 reaction equation
CS(C)=O.C(Cl)(=O)C(Cl)=O.[CH3:11][O:12][C:13]1[CH:41]=[CH:40][C:16]([CH2:17][O:18][C:19](=[O:39])[C@@H:20]2[CH2:24][C@@H:23]([OH:25])[CH2:22][N:21]2[C:26]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([N+:36]([O-:38])=[O:37])=[CH:32][CH:31]=2)=[O:27])=[CH:15][CH:14]=1.C(N(CC)CC)C>C(Cl)Cl>[CH3:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:17][O:18][C:19](=[O:39])[C@@H:20]2[CH2:24][C:23](=[O:25])[CH2:22][N:21]2[C:26]([O:28][CH2:29][C:30]2[CH:35]=[CH:34][C:33]([N+:36]([O-:38])=[O:37])=[CH:32][CH:31]=2)=[O:27])=[CH:40][CH:41]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 65578Oxalyl chlorideHCID 13504318trans-1-(p-nitrobenzyloxycarbonyl)-4-hydroxy-L-proline p-methoxybenzyl ester

Product 1

HCID 151163081-(p-nitrobenzyloxycarbonyl)-4-oxo-L-proline p-methoxybenzyl ester

Reagents, catalysts & solvents 1

HCID 6344
Dichloromethane
Solvent
4×

Procedure

A solution of 0.35 ml of dimethyl sulfoxide in 1 ml of dried methylene chloride was added dropwise to a solution of 0.2 ml of oxalyl chloride in 5 ml of dried methylene chloride at -60° to -70° C. Ten minutes later, 10 ml of a dried methylene chloride solution of 860 mg of trans-1-(p-nitrobenzyloxycarbonyl)-4-hydroxy-L-proline p-methoxybenzyl ester was added dropwise to the above mixture at a temperature of -50° C. or less, followed by stirring for 15 minutes. 1.01 g of triethylamine was then added dropwise thereto, and the resulting mixture was warmed to room temperature. The mixture was diluted with methylene chloride, washed with dilute hydrochloric acid aqueous solution and dried over sodium sulfate. The solvent was removed by distillation, and the residue was purified by silica gel column chromatography to yield 1-(p-nitrobenzyloxycarbonyl)-4-oxo-L-proline p-methoxybenzyl ester.

Workup

  1. washwashed with dilute hydrochloric acid aqueous solution
  2. dry with materialdried over sodium sulfate
  3. customThe solvent was removed by distillation
  4. customthe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-ac269d1fac6c4d10bdbd5349a81f09fd
Source dataset
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05122604

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes