HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Dimethyl 2-methyl-2-(4-nitrophenyl)malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dimethyl 2-(4-nitrophenyl)malonate | HCID 2764303 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dimethyl 2-methyl-2-(4-nitrophenyl)malonate | HCID 1485451 | 66.3% |
Reaction Steps
To a stirred solution of dimethyl 2-(4-nitrophenyl)malonate (10 g, 39.52 mmol, 1.0 eq) and K2CO3 (10.9 g 79.05 mmol 2.0 eq) in DMF (40 mL), was added methyl iodide (4.94 mL, 79.05 mmol 2.0 eq) at 0° C. and the mixture stirred at RT for 18 h. K2CO3 was filtered out and the filtrate concentrated under vacuum. The residue was diluted with water (80 mL) and extracted with EtOAc (2×80 mL). The organic layer was separated washed with brine solution, dried over anhydrous Na2SO4 and the solvent evaporated to get dimethyl 2-methyl-2-(4-nitrophenyl)malonate (7 g, 66%; TLC system: EtOAc/PE (3:7), Rf: 0.5.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946204B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-0ac5f0688225410bafab0b1d96e24146 |
| Source note | uspto-grants-2015_02 |