Trifluoroacetic acid → Trifluoroacetate

HRID 1447624Notes

Reaction equation

HRID 1447624 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

1-[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 1-(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-d3d79f88b7144acb8d93e4d68ed8494c
Source dataset
uspto-grants-1979_12
Patent number
US04177277

Reaction notes

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