HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399563Generated: October 31, 2026
Hydrochloric Acid → Dimethyl 2-acetyl-3-propylsuccinate
https://huagongshe.com/reaction/1399563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-bromovalerate | HCID 79071 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dimethyl 2-acetyl-3-propylsuccinate | HCID 86665649 | 55.9% |
Reaction Steps
To a solution of ethyl acetoacetate (64 mL; 504 mmol) in dry DMF (240 mL) under a nitrogen atmosphere was added potassium carbonate (69.6 g; 504 mmol), which has been dried at 120° C. for 12 h before its use. After stirring for 15 minutes at room temperature, ethyl 2-bromovalerate (81.6 mL; 480 mmol) was slowly added under nitrogen and the mixture was vigorously stirred at room temperature for 20 h. The reaction mixture was poured in water (240 mL) and neutralized by adding HCl 2N. The product was extracted with diethyl ether (2×240 mL) and the combined organic layers were dried over magnesium sulphate and concentrated under reduced pressure. The crude yellow oil was purified by distillation under reduced pressure (160° C./6 mbar) to give 61.8 g of the title compound as a colorless liquid (HPLC purity 60%). ESI/APCI(+): 259 (M+H);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906906B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-83a9736b9acd4fa48c4aa9e211b22c83 |
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| Source note | uspto-grants-2014_12 |
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