HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566184Generated: November 2, 2026
Pyridine → ethyl N-(4-bromo-5-ethoxy-2-fluorophenyl)carbamate
https://huagongshe.com/reaction/566184
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-Bromo-5-ethoxy-2-fluoroaniline | HCID 13281429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl N-(4-bromo-5-ethoxy-2-fluorophenyl)carbamate | HCID 21265588 | 96.3% |
Reaction Steps
Ethyl chloroformate (2.15 g) was added dropwise to a solution of 4-bromo-5-ethoxy-2-fluoroaniline (4.21 g) and pyridine (2.84 g) in methylene chloride (36 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, and the resulting crude crystals were crystallized from a mixed solvent of ethyl acetate and n-hexane (1:5 v/v) to obtain the objective ethyl N-(4-bromo-5-ethoxy-2-fluorophenyl)carbamate (5.30 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-296db66172274adf93bcc36a6c01abf3 |
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| Source note | uspto-grants-2001_01 |
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