Acetic Anhydride → HCID 53656353, compound

HRID 330088Notes

Reaction equation

HRID 330088 reaction equation
[F:1][C:2]1[C:15]([CH3:16])=[C:14]([F:17])[C:13]([F:18])=[CH:12][C:3]=1[C:4]([CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5].[CH:19]([O-])([O-])[O:20][CH2:21][CH3:22].C(OC(=O)C)(=O)C>>[F:1][C:2]1[C:15]([CH3:16])=[C:14]([F:17])[C:13]([F:18])=[CH:12][C:3]=1[C:4]([C:6](=[CH:19][O:20][CH2:21][CH3:22])[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5]

Participants

4

Reactant 3

HCID 7918Acetic AnhydrideHCID 14052572Ethyl 3-oxo-3-(2,4,5-trifluoro-3-methylphenyl)propanoateHCID 53630039Ethylorthoformate

Product 1

HCID 53656353HCID 53656353, compoundYield 100.1%

Procedure

A mixture of ethyl 2-(2,4,5-trifluoro-3-methylbenzoyl)acetate (3.0 g), ethyl orthoformate (2.6 g) and acetic anhydride (2.9 g) was stirred at 87° to 93° C. for 6 hours and then concentrated under reduced pressure to give the title compound (3.65 g) as orange oil.

Workup

  1. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-cc7552bf086b46a087303fa155ee615c
Source dataset
uspto-grants-1990_01
Patent number
US04894458

Reaction notes

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