HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Acetylamino-6-bromo-2-nitro-benzoic acid → Methyl 3-acetylamino-6-bromo-2-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Acetylamino-6-bromo-2-nitro-benzoic acid | HCID 11403903 | — |
| Reactant | trimethylsilyldiazomethane Et2O | HCID 23159941 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3-acetylamino-6-bromo-2-nitrobenzoate | HCID 11151255 | 66.4% |
Reaction Steps
To a mixed solution of 3-(acetylamino)-6-bromo-2-nitrobenzoic acid (2.00 g, 6.60 mmol) in methanol (20 mL) and tetrahydrofuran (5 mL) was added 2M trimethylsilyldiazomethane/diethyl ether solution (10.6 mL, 21.1 mmol) under ice-cooling, and the mixture was stirred at room temperature for 5 days. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=25/75→60/40) to give the title compound (1.39 g, yield 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247429B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-ab75b8843663424d92e2efdb870c0921 |
| Source note | uspto-grants-2012_08 |