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Acetic Anhydride → Ethyl 2-(2,4,5-trifluoro-6-methylbenzoyl)-3-ethoxyacrylate

HRID 1276
Notes
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Reaction equation

HRID 1276 reaction equation
[CH3:1][C:2]1[C:15]([F:16])=[C:14]([F:17])[CH:13]=[C:12]([F:18])[C:3]=1[C:4]([CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5].[C:19]([O:22][C:23](=O)C)(=O)[CH3:20].C(OC(OCC)OCC)C>>[CH3:1][C:2]1[C:15]([F:16])=[C:14]([F:17])[CH:13]=[C:12]([F:18])[C:3]=1[C:4]([C:6](=[CH:23][O:22][CH2:19][CH3:20])[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 7918Acetic AnhydrideHCID 31214Ethyl orthoformateHCID 14517129Ethyl (3,4,6-Trifluoro-2-methylbenzoyl)acetate

Product 1

HCID 54242925Ethyl 2-(2,4,5-trifluoro-6-methylbenzoyl)-3-ethoxyacrylateYield 90%

Procedure

To ethyl 2-methyl-3,4,6-trifluorobenzoylacetate (3.2 g) are added acetic anhydride (3.0 g) and triethoxymethane (2.7 g) and the mixture is refluxed for 1 hour. After concentrating, ethyl 2-(2-methyl-3,4,6-trifluorobenzoyl)-3-ethoxyacrylate (3.5 g) is obtained.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • temperaturethe mixture is refluxed for 1 hour
  • concentrationAfter concentrating
  • Sources & evidence

    ORD record
    ord-1c88fe3c527448899e928f57e94a62f9
    Source dataset
    uspto-grants-1998_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05723648

    Reaction notes

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