HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 2-methyl-6-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Methyl-2-nitrobenzoic acid | HCID 16097 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 2-methyl-6-nitrobenzoate | HCID 596057 | — |
Reaction Steps
To a solution of the 2-methyl-6-nitro-benzoic acid (5.6 g, 30.9 mmol, 1.0 eq, Aldrich) and acetone (100 mL) was added crushed K2CO3 (21.4 g, 154.6 mmol, 5 eq) and MeI (9.6 mL, 154.6 mmol, 5.0 eq.). The reaction was heated to reflux for 15 h then cooled to RT, filtered and concentrated in vacuo. The filtrate was dissolved in EtOAc, washed with H2O and brine, dried (MgSO4) and concentrated in vacuo to give the desired compound as a reddish-brown oil which upon standing at RT crystallized as tan needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07390820B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-ca3edb7fbf8848eeaa728149acea2bb2 |
| Source note | uspto-grants-2008_06 |