HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566194Generated: November 1, 2026
Pyridine → ethyl N-(5-allyloxy-4-bromo-2-fluorophenyl)carbamate
https://huagongshe.com/reaction/566194
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 5-Allyloxy-4-bromo-2-fluoroaniline | HCID 21265598 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl N-(5-allyloxy-4-bromo-2-fluorophenyl)carbamate | HCID 21265559 | 98.5% |
Reaction Steps
Ethyl chloroformate (5.97 g) was added dropwise to a solution of 5-allyloxy-4-bromo-2-fluoroaniline (12.3 g) and pyridine (7.90 g) in methylene chloride (100 ml) at 0° C., and the mixture was stirred at 10° C. for 3 hours. After the reaction, this was extracted with methylene chloride, then washed with diluted hydrochloric acid and an aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. Then, methylene chloride was distilled off to obtain to the objective ethyl N-(5-allyloxy-4-bromo-2-fluorophenyl)carbamate (15.67 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174839B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-fc87c21c7daf4bdfac9311e38a6a25ec |
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| Source note | uspto-grants-2001_01 |
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