HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Methoxy-2-methyl-7-nitro-2,3-dihydro-isoindol-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxy-2-methyl-7-nitro-2,3-dihydro-isoindol-1-one | HCID 59849205 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Methoxy-2-methyl-7-nitro-2,3-dihydro-isoindol-1-one | HCID 59849179 | 50% |
Reaction Steps
A mixture of 4-Hydroxy-2-methyl-7-nitro-2,3-dihydro-1H-isoindol-1-one (Compound 205C, 50.0 mg, 0.240 mmol), potassium carbonate (49.8 mg, 0.360 mmol) in DMF (2 mL, 20 mmol) was treated with methyl iodide (22.4 μL, 0.360 mmol) and allowed to stir at room temperature overnight. The reaction was poured into EtOAc and washed with water and brine and the crude material was purified using an ISCO Combiflash unit (MeOH in DCM: 0-1%) to obtain the title product as a solid. (27 mg, 50% yield). 1H NMR (400 MHz, CD3OD) δ=3.17 (s, 3H), 4.02 (s, 3H), 4.44 (s, 2H), 7.27 (d, J=8.8 Hz, 1H), 7.94 (d, J=8.8 Hz, 1H). MS (ES+): m/z 223.19 (100) [MH+]; HPLC: tR=0.76 min (UPLC, analytical).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399433B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-90663d918e084cac90d3edd9d7a229d7 |
| Source note | uspto-grants-2013_03 |