HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → Methyl 2-acetylamino-4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Benzoic acid, 2-(acetylamino)-4-nitro- | HCID 70373 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Benzene methanol | HCID 21927730 | — |
| Product | Methyl 2-acetylamino-4-nitrobenzoate | HCID 12399497 | 97.1% |
Reaction Steps
To a stirred solution of 2-acetylamino-4-nitrobenzoic acid (1.28 g, 5.71 mmol) in benzene-MeOH (4:1, v/v, 25 mL), was added trimethylsilyldiazomethane (2.0 M solution in n-hexane, 4.28 ml, 8.56 mmol) at 0° C. The stirring was continued for 18 hours at rt. The reaction was poured into hexane, and the resulting precipitate was collected by filtration to give methyl 2-acetylamino-4-nitrobenzoate (1.32 g, 97%) as a white solid; mp no data; 1H-NMR (400 MHz, CDCl3) δ2.30 (s, 3 H), 4.00 (s, 3 H), 7.88 (m, 1 H), 8.18 (dd, J=2.0 Hz, 8.8 Hz, 1 H), 9.60 (t, J=2.2 Hz, 1 H), 11.10 (s, 1 H); MS (ESI) m/z 238 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06756378B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-8abce11d590a4598a349418f8037dc9f |
| Source note | uspto-grants-2004_06 |