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Trifluoroacetic acid → HCID 86735587, compound

HRID 1679785
Notes
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Reaction equation

HRID 1679785 reaction equation
[CH3:1][O:2][C:3](=[O:22])[CH2:4][NH:5][C:6](=[O:21])[C@H:7]([CH3:20])[NH:8][C:9](=[O:19])[CH2:10][NH:11]C(OC(C)(C)C)=O.[F:23][C:24]([F:29])([F:28])[C:25]([OH:27])=[O:26]>>[F:23][C:24]([F:29])([F:28])[C:25]([OH:27])=[O:26].[CH3:1][O:2][C:3](=[O:22])[CH2:4][NH:5][C:6](=[O:21])[C@H:7]([CH3:20])[NH:8][C:9](=[O:19])[CH2:10][NH2:11]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6422Trifluoroacetic acidHCID 86735588HCID 86735588, compound

Product 1

HCID 86735587HCID 86735587, compound

Conditions

Temperature
0 °C

Procedure

Boc-Gly-Ala-Gly-OMe (6.4 g, 20.1 mmoles, described in Example 2) is dissolved in cold (ice bath) trifluoroacetic acid (120 ml) and the solution stirred at 0° C for 1 hr. The solvent is evaporated, the residue dissolved in methanol and the product precipitated with the addition of diethyl ether. The precipitiate is collected to give the title compound.

Workup

  1. customThe solvent is evaporated
  2. dissolutionthe residue dissolved in methanol
custom
the product precipitated with the addition of diethyl ether
  • customThe precipitiate is collected
  • Sources & evidence

    ORD record
    ord-ecc9aa2f6fb04a0481ac1e5b0c1ae579
    Source dataset
    uspto-grants-1978_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04081530

    Reaction notes

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    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes