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Acetic Anhydride → HCID 13893921, compound

HRID 1381375
Notes
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Reaction equation

HRID 1381375 reaction equation
[OH:1][C:2]1[C:6](=[O:7])[O:5][CH:4]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])[C:3]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[C:19](OC(=O)C)(=[O:21])[CH3:20]>N1C=CC=CC=1>[C:19]([O:1][C:2]1[C:6](=[O:7])[O:5][CH:4]([CH2:8][CH2:9][C:10]([OH:12])=[O:11])[C:3]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)(=[O:21])[CH3:20]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7918Acetic AnhydrideHCID 128356WF 3681

Product 1

HCID 13893921HCID 13893921, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

3-(4-Hydroxy-5-oxo-3-phenyl-2,5-dihydro-2-furyl)-propionic acid (100 mg) was dissolved in pyridine (2 ml), and acetic anhydride (1 ml) was added. The mixture was allowed to stand overnight. The excess reagent and solvent were removed by distillation under reduced pressure, and the residue was dried to give 3-(4-acetoxy-5-oxo-3-phenyl-2,5-dihydro-2-furyl)propionic acid (116 mg) as an oil.

Workup

  • customThe excess reagent and solvent were removed by distillation under reduced pressure
  • customthe residue was dried
  • Sources & evidence

    ORD record
    ord-5b7d2907bcc04a978f8b91fd38a09b55
    Source dataset
    uspto-grants-1986_04
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04585789

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes