HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232174Generated: October 31, 2026
Triethylamine → Phenyl (2-chloropyridin-4-yl)carbamate
https://huagongshe.com/reaction/2232174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 2-Chloropyridin-4-amine | HCID 84432 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenyl (2-chloropyridin-4-yl)carbamate | HCID 21247422 | 37.7% |
Reaction Steps
Under a dry nitrogen atmosphere a solution of 12.0 ml (0.096 mole) of phenyl chloroformate in 300 ml of methylene chloride was added dropwise to a cold (0° C.) stirred solution of 10.2 g (0.079 mole) of 4-amino-2-chloropyridine and 16.5 ml (0.12 mole) of triethylamine in 300 ml of methylene chloride. After complete addition the reaction mixture was allowed to come to room temperature and stirred at room temperature for approximately 18 hours. The mixture was washed with three 100 ml portions of water followed by 100 ml of an aqueous saturated sodium chloride solution. The washed mixture was dried over anhydrous magnesium sulfate and filtered. The filtrate was subjected to column chromatography on silica gel, eluted with acetone:methylene chloride (4:96), to yield 7.4 g of phenyl N-(2-chloro-4-pyridinyl)carbamate as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04787931 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-dd8c3fba377e42e9b0879aa7fba34983 |
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| Source note | uspto-grants-1988_11 |
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