HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21353Generated: October 25, 2026
Methyl chloroformate → 4-Methoxycarbonyloxy-3-fluorobenzoic acid
https://huagongshe.com/reaction/21353
Participants
| Role | Name | HCID | Charge |
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| 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 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 |
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| Patent number | US05422037 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-6e7542b50106400f83a25fb640e5a93d |
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| Source note | uspto-grants-1995_06 |
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