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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-(3,5-Dichloro-4-methylphenyl)ethan-1-one | HCID 13713529 | — |
| Reactant | Glyoxylic acid, monohydrate | HCID 15620607 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(3,5-Dichloro-4-methylphenyl)-4-oxobut-2-enoic acid | HCID 54534153 | 80.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04603201 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-d3b7260e801f42c58fc0bfd7af3da17e |
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| Source note | uspto-grants-1986_07 |
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