HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 4-chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoic acid | HCID 68736172 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoate | HCID 68737379 | 90% |
Reaction Steps
A mixture of 4-chloro-2-[(3-chloropropyl)amino]-3-nitrobenzoic acid (150 mg, 0.512 mmol), methyl iodide (0.0319 mL, 0.512 mmol) and potassium carbonate (70.8 mg, 0.512 mmol) in N,N-dimethylformamide (1.5 mL) was stirred at room temperature for 12 h. After addition of ethyl acetate, the resultant mixture was washed with water and brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on NH silica gel eluting with a 5% ethyl acetate/n-hexane mixture to afford a yellow oil (141 mg, 0.459 mmol, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901141B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-ca10df22104d40c29db6c322f0aa5b36 |
| Source note | uspto-grants-2014_12 |