HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111100Generated: October 30, 2026
Ethyl 2-(4-chlorophenoxy)acetoacetate → Ethyl 5-chloro-3-methylbenzofuran-2-carboxylate
https://huagongshe.com/reaction/1111100
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-(4-chlorophenoxy)acetoacetate | HCID 15678688 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 5-chloro-3-methylbenzofuran-2-carboxylate | HCID 15643819 | 65% |
Reaction Steps
Ethyl 2 (4-chlorophenoxy)acetoacetate (90.3 g, 0.353 mol) was added dropwise to sulfuric acid (240 ml) stirred at 0° C. The resulting suspension was stirred at 0° C. for 3.5 hours, poured onto crushed ice and the mixture stirred for 0.5 hours. The mixture was extracted with toluene and the organic phase was washed with 5% sodium bicarbonate and water. The organic phase was dried with magnesium sulfate, filtered and concentrated. The crude product was recrystallized from cyclohexane to give 54.5 g (65%) of ethyl 5-chloro-3-methyl-2-benzofuran carboxylate: mp 80°-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04978660 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-f95b56b889214ce3af0583ae4040572d |
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| Source note | uspto-grants-1990_12 |
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