HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658458Generated: October 30, 2026
Methyl chloroformate → Methyl 2-cyanobenzoate
https://huagongshe.com/reaction/1658458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Phthalamic acid | HCID 6957 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-cyanobenzoate | HCID 582554 | — |
Reaction Steps
Phthalamic acid (240 g, 1.37 moles) in methylenechloride (1.7 l) was stirred and cooled to <5° in an ice bath. Triethylamine (244 ml, 176 g, 1.74 moles) was added and a clear solution was obtained. Methyl chloroformate (200 g, 163 ml, 2.1 moles) was added at such a rate that the temperature did not exceed 5°. As the addition continued, triethylamine hydrochloride precipitated and carbon dioxide was evolved. On completion of the addition, the ice bath was removed and stirring was continued for 12-20 hrs. at room temperature. Triethylamine hydrochloride was removed by filtration and the methylene chloride evaporated. The residue was dissolved in ether (2 l), and this ether solution washed with water, dried over anhydrous sodium sulfate and evaporated. Distillation under reduced pressure gave methyl 2-cyanobenzoate, b.p. 125° at 2.5 mm, 215 g (97%), a solid at room temperature, M.P. 45°-6°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03964896 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-93126227cf7d4a7e8f7d3b784522cee2 |
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| Source note | uspto-grants-1976_06 |
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