HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl p-toluenesulfonate → Methyl 2-amino-6-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl p-toluenesulfonate | HCID 6645 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-6-nitro-benzoic acid | HCID 95795 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-amino-6-nitrobenzoate | HCID 596477 | 59.4% |
Reaction Steps
A mixture of 2-amino-6-nitrobenzoic acid (11.9 g, 65.3 mmol), methyl p-toluenesulfonate (15.1 g, 81.1 mmol) and triethylamine (6.60 g, 65.3 mmol) in DMF (170 ml) was stirred under N2 at 60° for 18 hours. After removing DMF at 60° and 0.2 mm pressure, the residue was dissolved in ETOAc and washed with a saturated solution of NaHCO3 followed by a saturated aqueous solution of NaCl. The EtOAc extract was dried (Na2SO4), filtered and concentrated under reduced pressure. Flash chromatography over silica gel and elution with 50% toluene-50% CHCl3 gave methyl 2-amino-6-nitrobenzoate (7.6 g, 59.4%), m.p. 105°-107°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04647588 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-c58b0cae364846e7812e6f98f7bce7fd |
| Source note | uspto-grants-1987_03 |