HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl chloroformate → 4-Methoxycarbonyloxy-3-fluorobenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Fluoro-4-hydroxybenzoic acid | HCID 160456 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Methoxycarbonyloxy-3-fluorobenzoic acid | HCID 53762941 | — |
Reaction Conditions
| Temperature | -20 °C |
|---|
Reaction Steps
4-methoxycarbonyloxy-3-fluorobenzoic acid (VI) was synthesized from 3-fluoro-4-hydroxybenzoic acid (V) by reaction of the latter with methyl chloroformate. NaOH (90 mmol) and 3-fluoro-4-hydroxybenzoic acid (30 mmol) were dissolved in water (80 ml) and cooled to -20° C. Methyl chloroformate (45 mmol) was added dropwise to the mixture. The mixture was then stirred with a magnetic stir bar at 5° C. for four hours and left overnight in the refrigerator. The mixture was then acidified to pH 5 to precipitate 4-methoxycarbonyloxy-3-fluorobenzoic acid. The precipitates were filtered and crystallized from acetonitrile to afford the clean product, 4-methoxycarbonyloxy -3-fluorobenzoic acid (VI), in a 77% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05180520 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-a2d77263d4fb44438e5e1929040d716a |
| Source note | uspto-grants-1993_01 |