HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806936Generated: November 3, 2026
Pyridine → 2-(1-Ethyl-propylidene)-malonic acid dimethyl ester
https://huagongshe.com/reaction/1806936
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ethyl ketone | HCID 7288 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-Ethyl-propylidene)-malonic acid dimethyl ester | HCID 85648770 | 46.6% |
Reaction Steps
Step A To a solution of dimethyl malonate (10 g, 75 mmol), 3-pentanone (6.5 g, 75 mmol) and pyridine (7.9 g, 100 mmol) in anhydrous tetrahydrofuran (300 mL) at 0° C. was added a dichloromethane solution (1 M) of TiCl4 (100 mL, 100 mmol) during a period of 1 h. After the addition was finished, the reaction mixture was gradually warmed room temperature and stirred for 18 h. Water was added to quench the reaction. The mixture was extracted with ethyl ether. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layers were combined, concentrated. The residue was purified by chromatography (EtOAc:hexanes=1:20) to give 2-(1-ethyl-propylidene)-malonic acid dimethyl ester as a light yellow oil (7 g, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354444B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-b3bda9c158c3401ab88cb01c0c8f55b5 |
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| Source note | uspto-grants-2013_01 |
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