HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807019Generated: October 25, 2026
Pyridine → 2-[1-(5-Methyl-furan-2-yl)-ethylidene]-malonic acid dimethyl ester
https://huagongshe.com/reaction/1807019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | 2-Acetyl-5-Methylfuran | HCID 14514 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[1-(5-Methyl-furan-2-yl)-ethylidene]-malonic acid dimethyl ester | HCID 14357288 | 32% |
Reaction Steps
Step A To a solution of dimethyl malonate (6.5 g, 49 mmol), 2-acetyl-5-methylfuran (6.1 g, 49 mmol) and pyridine (16 g, 200 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=1:10) to give 2-[1-(5-methyl-furan-2-yl)-ethylidene]-malonic acid dimethyl ester as a yellow oil (3.7 g, 32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08354444B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-62edc8134eb2433e82f62edd527c5580 |
|---|
| Source note | uspto-grants-2013_01 |
|---|