HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-2-nitrotoluene → Benzoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-2-nitrotoluene | HCID 123546 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 4-Bromo-2-nitrobenzoic acid | HCID 3774467 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzoic Acid | HCID 243 | 22% |
Reaction Steps
4-Bromo-2-nitrobenzoic acid. A mixture of 4-bromo-2-nitrotoluene (5.0 g, 23 mmol), KMnO4 (10.9 g, 69 mmol), and water (250 mL) was heated at reflux overnight in a 1 L round-bottom flask fitted with a reflux condenser. The brown suspended MnO2 was removed by filtration through a pad of diatomaceous earth. The filter cake was washed with water. The basic filtrate was acidified to pH˜1 with concentrated HCl and extracted with EtOAc (3×300 mL). The combined organic layers were dried (MgSO4) and concentrated in vacuo to provide pure benzoic acid (1.22 g, 22%). 1H NMR (400 MHz, CD3OD): 8.07 (d, J=1.9 Hz, 1H), 7.85 (dd, J=8.2, 1.9 Hz, 1H), 7.65 (d, J=8.2 Hz, 1H). MS (ESI): neg. ion m/z 244 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241759B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-8e4f31d5872e4da985b4814ca6219aa8 |
| Source note | uspto-grants-2007_07 |