1-(2-ethoxycarbonylpropanoyl)-L-proline → 1-(2-carboxypropanoyl)-L-proline

HRID 2083709Notes

Reaction equation

HRID 2083709 reaction equation
C([O:3][C:4]([CH:6]([CH3:17])[C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8])=[O:5])C>[OH-].[Na+].CO>[C:4]([CH:6]([CH3:17])[C:7]([N:9]1[CH2:16][CH2:15][CH2:14][C@H:10]1[C:11]([OH:13])=[O:12])=[O:8])([OH:5])=[O:3]

Participants

4

Reactant 1

HCID 536785471-(2-ethoxycarbonylpropanoyl)-L-proline

Product 1

HCID 542987211-(2-carboxypropanoyl)-L-proline

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 14798Sodium HydroxideSolvent

Procedure

1-(2-Ethoxycarbonylpropanoyl)-L-proline (4.1 g.) is dissolved in a mixture of N sodium hydroxide (51 ml.) and methanol (51 ml.). The solution is kept at room temperature for 6 hours and then concentrated to half volume in vacuo. Ion exchange resin (Dowex 50) (50 ml.) is added and the suspension applied to a column of 150 ml. of the same resin. The fractions containing the desired material (carboxyl reagent positive) are pooled and freeze dried to obtain to obtain 1-(2-carboxypropanoyl)-L-proline, yield 1.5 g.

Workup

  1. concentrationconcentrated to half volume in vacuo
  2. additionIon exchange resin (Dowex 50) (50 ml.) is added
  3. additionThe fractions containing the desired material (carboxyl reagent positive)
  4. customfreeze dried
  5. customto obtain

Sources & evidence

ORD record
ord-4607ef9c0688414fbca0beefe1d1d7e7
Source dataset
uspto-grants-1978_04
Patent number
US04086338

Reaction notes

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