HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Methyl 3-amino-5-morpholino-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-amino-5-chloro-2-nitrobenzoate | HCID 12165619 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-amino-5-morpholino-2-nitrobenzoate | HCID 58278827 | 46.3% |
Reaction Steps
A mixture of combined batches of methyl 3-amino-5-chloro-2-nitrobenzoate (39 g), morpholine (29.5 g) and K2CO3 (47 g) was stirred in DMF (200 ml) at 110° C. for 5 h. The mixture was cooled to room temperature and poured into water (1 L). It was extracted with EtOAc (500 mL×3). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in-vacuo to afford the desired product as a yellow solid (22 g, yield 46%). 1H NMR (300 MHz, CDCl3): δ ppm 3.31 (t, 4H, J=4.8 Hz), 3.82 (t, 4H, J=4.8 Hz), 3.89 (s, 3H), 6.03 (d, 1H, J=2.4 Hz), 6.34 (d, 1H, J=2.4 Hz); LC-MS: m/e=282 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541411B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-51137de1b080429ba17170c4a9760189 |
| Source note | uspto-grants-2013_09 |