HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-4-nitrotoluene → 2-Fluoro-4-nitrobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-4-nitrotoluene | HCID 74025 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Benzyl 2-fluoro-4-hydroxybenzoate | HCID 18006244 | — |
| Product | 2-Fluoro-4-nitrobenzoic acid | HCID 302679 | — |
Reaction Steps
This was prepared as described above in Example 33 except that benzyl 2-fluoro-4-hydroxybenzoate (prepared from 2-fluoro-4-nitrotoluene by oxidation with KMnO4 to give 2-fluoro-4-nitrobenzoic acid, followed by catalytic reduction to give 4-amino-2-fluorobenzoic acid, followed by diazotization/hydrolysis to give 4-hydroxy-2-fluorobenzoic acid which was converted to benzyl 2-fluoro-4-hydroxybenzoate in a fashion analogous to that described in Example 23) was used as starting material in place of benzyl 2-chloro-4-hydroxybenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05229381 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-288cd257beaf412d9fc874a8c02af4b3 |
| Source note | uspto-grants-1993_07 |