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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746269Generated: October 30, 2026

Diisopropyl Ether → 4-(3,5-Dichloro-4-methylphenyl)-4-oxobut-2-enoic acid

https://huagongshe.com/reaction/746269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropyl EtherHCID 7914—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(3,5-Dichloro-4-methylphenyl)ethan-1-oneHCID 13713529—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
CatalystSulfuric AcidHCID 1118—
SolventAcetic AcidHCID 176—
Product4-(3,5-Dichloro-4-methylphenyl)-4-oxobut-2-enoic acidHCID 5453415380.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

10.2 g (0.1 mole) of acetic anhydride were added to 9.3 g (0.1 mole) of glyoxylic acid monohydrate and the mixture was heated, with stirring, on an oil bath at 60° C. for 10 minutes to obtain a homogeneous solution. To this solution were added, in turn, 20.3 g (0.1 mole) of 3,5-dichloro-4-methylacetophenone, prepared as described in step (a) above, 28.8 g of acetic acid and a catalytic amount (300 mg) of concentrated sulphuric acid, whilst ice-cooling. The mixture was then heated, with stirring, on an oil bath at 105°-110° C. for 2 hours, after which it was cooled and 100 ml of diisopropyl ether were added. The mixture was stirred and the resulting crystals were collected by filtration and washed first with water and then with a small amount of diisopropyl ether, after which they were dried to give 20.8 g (yield 80.3%) of the desired 4-(3,5-dichloro-4-methylphenyl)-4-oxo-2-butenoic acid, melting at 206°-216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04603201
Source datasetuspto-grants-1986_07
ORD IDord-d3b7260e801f42c58fc0bfd7af3da17e
Source noteuspto-grants-1986_07