Trifluoroacetic acid → Trifluoroacetate

HRID 1762521Notes

Reaction equation

HRID 1762521 reaction equation
C([O:5][C:6](=[O:36])[C@@H:7]1[CH2:11][CH2:10][CH2:9][N:8]1[C:12](=[O:35])[CH:13]([CH2:30][S:31][C:32](=[O:34])[CH3:33])[CH2:14][CH2:15][CH2:16][NH:17]C(OCC1C=CC(OC)=CC=1)=O)(C)(C)C.[F:37][C:38]([F:43])([F:42])[C:39]([OH:41])=[O:40]>C1(OC)C=CC=CC=1>[C:32]([S:31][CH2:30][CH:13]([CH2:14][CH2:15][CH2:16][NH2:17])[C:12]([N:8]1[CH2:9][CH2:10][CH2:11][C@H:7]1[C:6]([OH:36])=[O:5])=[O:35])(=[O:34])[CH3:33].[F:37][C:38]([F:43])([F:42])[C:39]([O-:41])=[O:40]

Participants

5

Reactant 2

HCID 6422Trifluoroacetic acidHCID 228053291-[2-Acetylthiomethyl-5-(p-methoxybenzyloxycarbonylamino)pentanoyl]-L-proline tert-butyl ester

Product 2

HCID 84468TrifluoroacetateHCID 14181479HCID 14181479, compound

Reagents, catalysts & solvents 1

HCID 7519AnisoleSolvent

Procedure

N-[2-Acetylthiomethyl-5-(p-methoxybenzyloxycarbonylamino)pentanoyl]-L-proline tert-butyl ester (2 g.) is dissolved in a mixture of trifluoroacetic acid (15 ml.) and anisole (6 ml.). The solution is stored at room temperature for one hour, the solvents are removed in vacuo and the residue is precipitated from ethyl acetate-ether to yield N-(2-acetylthiomethyl-5-aminopentanoyl)-L-proline, trifluoroacetate.

Workup

  1. customthe solvents are removed in vacuo
  2. customthe residue is precipitated from ethyl acetate-ether

Sources & evidence

ORD record
ord-095b32edd2674233b35a44a31a746d52
Source dataset
uspto-grants-1989_05
Patent number
US04833152

Reaction notes

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