Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653201Generated: October 28, 2026

Potassium Hydroxide → 4-(2',5'-Dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acid

https://huagongshe.com/reaction/653201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2,5-Dimethoxy-3,4,6-trimethylbenzaldehydeHCID 2752605—
ReactantSodium pyruvateHCID 23662274—
SolventMethanolHCID 887—
Product4-(2',5'-Dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acidHCID 54412915100%

Reaction Steps

A suspension of 3.7 g (17.6 mmol) of 2,5-dimethoxy-3,4,6-trimethylbenzaldehyde and 5.0 g (53.2 mmol) of sodium pyruvate in 20 ml of methanol is treated with 0.1 g (1.8 mmol) of potassium hydroxide and the mixture is subsequently heated at reflux for 5 hours, whereby a yellow solution is obtained. The reaction mixture is poured on to ice-water and the resulting 4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acid is precipitated by the addition of sulphuric acid while stirring. The suspension is stirred for 1 hour, filtered, the filter residue is washed with water and dried. In this manner there are obtained 4.9 g of 4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-keto-3-butenoic acid in the form of a yellow powder of melting point 126°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04675421
Source datasetuspto-grants-1987_06
ORD IDord-1232696aa15541f8873a7e5dfffd322e
Source noteuspto-grants-1987_06