HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18964Generated: October 26, 2026
Ethyl Acetoacetate → 3-Chloro-but-2-enoic acid ethyl ester
https://huagongshe.com/reaction/18964
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Chloro-but-2-enoic acid ethyl ester | HCID 282835 | 83% |
Reaction Steps
To a stirred mixture of ethyl acetoacetate (15.0 g, 0.12 mol) in petroleum ether (30 mL) under a nitrogen atmosphere was added phosphorus pentachloride (12.7 g, 0.06 mol) gradually. After addition was complete the mixture was stirred at 25° C. for 1 h. Upon completion of the reaction water (50 mL) was added in small portions, transferred to a separatory funnel and the layers separated, followed by washing the aqueous layer with petroleum ether (2×50 mL). The combined petroleum ether extracts were washed with a 20% potassium carbonate solution, followed by a saturated sodium chloride solution and dried over magnesium sulfate. The combined organic layers were concentrated to give a yellow oil. Distillation of the residue yielded 3-chloro-but-2-enoic acid ethyl ester (7.4 g 43%) as a clear oil: LR-ES-MS m/z calculated for C6H9ClO2 [M]+ 148, observed [M+H]+ 149.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741327B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-e6036ef11aa9408e8fa664960532b4d3 |
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| Source note | uspto-grants-2010_06 |
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