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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259617Generated: November 1, 2026

Vanillin → 5(4H)-Oxazolone, 4-((4-(acetyloxy)-3-methoxyphenyl)methylene)-2-methyl-

https://huagongshe.com/reaction/259617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVanillinHCID 1183—
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetylglycineHCID 10972—
ReactantSodium AcetateHCID 517045—
Product5(4H)-Oxazolone, 4-((4-(acetyloxy)-3-methoxyphenyl)methylene)-2-methyl-HCID 2754298—

Reaction Conditions

Temperature0 °C

Reaction Steps

152 g (1mol) of 4-hydroxy-3-methoxy-benzaldehyde, 41 g of sodium acetate, 80 g of N-acetylglycine and 242 g of acetic anhydride are heated together for 30 minutes to 100° C. and then for 21/2 hours to the refluxing temperature. The resulting solution is cooled to 0° C. and the crystals which have separated out are filtered off and washed with water. The crude 2-methyl-4-(3-methoxy-4-acetoxy-benzylidene)-5(4H)-oxazolone thus obtained is heated to the boil with 1,400 ml of acetone and 545 ml of water for 15 hours under a reflux condenser. Thereafter, the acetone is largely distilled off, whereupon the product crystallises out. After filtration, and washing with acetone, 4-acetoxy-α-acetylamino-3-methoxycinnamic acid of melting point 205°-206° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04038414
Source datasetuspto-grants-1977_07
ORD IDord-320f9b6658b2486faea4de9be3a5b2f0
Source noteuspto-grants-1977_07