HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 2-[(4-amino-3-nitrophenyl)carbonyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-(4-Amino-3-nitrobenzoyl)benzoic acid | HCID 2797522 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-[(4-amino-3-nitrophenyl)carbonyl]benzoate | HCID 14994663 | — |
Reaction Steps
A solution of 2-[(4-amino-3-nitrophenyl)carbonyl]benzoic acid (10 g, 35 mmol) in DMF (50 mL) was treated with cesium carbonate (23 g, 70 mmol) followed by iodomethane (2.2 mL, 35 mmol). The mixture was stirred at rt for 1 h, after which time 50 mL of water was added. A yellow precipitate formed. The solid was collected by filtration, rinsed with water, and dried in vacuo. Desired methyl 2-[(4-amino-3-nitrophenyl)carbonyl]benzoate was obtained as a yellow solid (8.36 g, 27.8 mmol, 80% yield). 1H NMR (400 MHz, d6-DMSO): 8.12 (br s, 2H), 8.10 (d, 1H), 7.78-7.75 (m, 2H), 7.70 (m, 1H), 7.48 (dd, 1H), 7.10 (d, 1H), 3.64 (s, 3H); MS (EI) for C15H12N2O5: 323 (MNa+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697737B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-0ba018c9dfd1464eabb076f08dccc258 |
| Source note | uspto-grants-2014_04 |