HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diflunisal → 2,4-Difluoro-1,1'-biphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diflunisal | HCID 3059 | — |
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2,4-Difluoro-1,1'-biphenyl | HCID 169974 | — |
Reaction Steps
5-(2,4-difluorophenyl)salicylic acid, an anti-inflammatory, anti-pyretic, analgesic agent is prepared by: (1) diazotizing 2,4-difluoroaniline in the presence of benzene to yield 2,4-difluorobiphenyl; (2) Friedel-Crafts acylation to produce 2',4'-difluoro-4-alkanoylbiphenyl; (3) oxidation of the alkanoyl group to produce 2',4'-difluoro-4-alkanoyloxybiphenyl; (4) hydrolysis of the alkanoyl group to produce 4-(2,4-difluorophenyl)phenol; and (5) Kolbe-Schmitt carboxylation to produce the final product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225730 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-7705dc1856f64654a33eddcb916b1931 |
| Source note | uspto-grants-1980_09 |