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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413656Generated: October 26, 2026

Ethylamine → N-(2-methoxyethyl)-N-ethylcarbamoyl chloride

https://huagongshe.com/reaction/1413656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantPhosgeneHCID 6371—
ReactantSodium HydroxideHCID 14798—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantN-(2-Methoxyethyl)ethylamineHCID 546877—
SolventDiethyl EtherHCID 3283—
ProductN-(2-methoxyethyl)-N-ethylcarbamoyl chlorideHCID 12238060—

Reaction Steps

Novel intermediate compounds used in the preparation described above were prepared as follows. N-ethyl-N-2-methoxyethylamine, b.p. 115°-116° C., was prepared by reaction of 3 molecular proportions of ethylamine with 1 molecular proportion of 1-bromo-2-methoxyethane in aqueous solution containing 1 equivalant of sodium hydroxide at 30°-50° C. To a stirred solution of 89.1 g. phosgene in 500 ml. dry ether at -20° C. was added a solution of 30.9 g. N-ethyl-N-2-methoxyethylamine in 50 ml. dry ether, maintaining the temperature of the reaction mixture at -20° C. The stirred mixture was then allowed to warm to room temperature during 1 hour. The reaction mixture was filtered and the filtrate evaporated in vacuo below 25° C. to remove the solvent and give the product, N-(2-methoxyethyl)-N-ethylcarbamoyl chloride as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251262
Source datasetuspto-grants-1981_02
ORD IDord-d23cd4887ff7408983a0b0e4c727b1e3
Source noteuspto-grants-1981_02