1-(2-ethoxycarbonylpropanoyl)-L-proline tert.-butyl ester → 1-(2-ethoxycarbonylpropanoyl)-L-proline

HRID 2083708Notes

Reaction equation

HRID 2083708 reaction equation
C([O:5][C:6](=[O:21])[C@@H:7]1[CH2:11][CH2:10][CH2:9][N:8]1[C:12](=[O:20])[CH:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH3:14])(C)(C)C>FC(F)(F)C(O)=O>[CH2:18]([O:17][C:15]([CH:13]([CH3:14])[C:12]([N:8]1[CH2:9][CH2:10][CH2:11][C@H:7]1[C:6]([OH:21])=[O:5])=[O:20])=[O:16])[CH3:19]

Participants

3

Reactant 1

HCID 706103371-(2-ethoxycarbonylpropanoyl)-L-proline tert.-butyl ester

Product 1

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

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Procedure

The ester obtained in Example 2 (5.9 g.) is dissolved in trifluoroacetic acid, the solution is kept at room temperature for one hour, and then concentrated to dryness in vacuo. The residue is dissolved in a mixture of ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous phase is acidified and extracted with ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate and concentrated to dryness in vacuo to obtain 1-(2-ethoxycarbonylpropanoyl)-L-proline, yield 4.1 g.

Workup

  1. concentrationconcentrated to dryness in vacuo
  2. dissolutionThe residue is dissolved in a mixture of ethyl acetate and saturated aqueous sodium bicarbonate
  3. extractionextracted with ethyl acetate
  4. dry with materialThe ethyl acetate layer is dried over magnesium sulfate
  5. concentrationconcentrated to dryness in vacuo

Sources & evidence

ORD record
ord-ca77abe928514539bcd78111f89be966
Source dataset
uspto-grants-1978_04
Patent number
US04086338

Reaction notes

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