HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 13601672, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | (E)-4-(3,4-dichlorophenyl)-4-oxo-but-2-enoic acid | HCID 6172511 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Product | HCID 13601672 | HCID 13601672 | 86% |
Reaction Steps
To an ice cooled solution of (E)-4-(3',4'-dichlorophenyl)-4-oxo-2-butenoic acid (2.4 g, 0.01 mol) in dry DMF (80 mL), DBU (1.5 mL, 0.01) was added dropwise on stirring, under nitrogen atmosphere. To the resulting stirred solution iodomethane (3.1 mL, 0.05 mol) dissolved in dry DMF (20 mL) was added dropwise over 20 min. The resulting solution was stirred at 0° C. for 1 hour and 3 hours at room temperature. The resulting reaction mixture was poured into ice-water on stirring, and the precipitate was filtered, washed with water and then with hexane. Recrystallization from diisopropyl ether/hexane provided the pure ester (2.2 g, 86%), pale yellow needles, mp. 108-109°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06048896 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-8a990e93bfea45e3a99a2b7df774c564 |
| Source note | uspto-grants-2000_04 |