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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597652Generated: October 29, 2026

Acetic Anhydride → 2-Methyl-4-(4-acetoxy-3-allyl-benzylidene)-5(4H)-oxazolone

https://huagongshe.com/reaction/597652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetylglycineHCID 10972—
ReactantSodium AcetateHCID 517045—
Reactant3-Allyl-4-hydroxybenzaldehydeHCID 4729014—
Product2-Methyl-4-(4-acetoxy-3-allyl-benzylidene)-5(4H)-oxazoloneHCID 53677355—

Reaction Conditions

Temperature0 °C

Reaction Steps

40.5 g (0.25 mol) of 3-allyl-4-hydroxy-benzaldehyde, 10.3 g of sodium acetate, 19.9 g of N-acetylglycine and 63.5 g of acetic anhydride are together heated for 30 minutes to 100°C and then for 21/2 hours to the reflux temperature. The resulting solution is cooled to 0°C and the crystals which have separated out are filtered off, washed with water, dried in a vacuum desiccator and finally recrystallised from carbon tetrachloride. 2-Methyl-4-(4-acetoxy-3-allyl-benzylidene)-5(4H)-oxazolone of melting point 108°-109°C is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014920
Source datasetuspto-grants-1977_03
ORD IDord-97f9d10739114340918dadef831fe861
Source noteuspto-grants-1977_03