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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | N-(2-Methoxyethyl)ethylamine | HCID 546877 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(2-methoxyethyl)-N-ethylcarbamoyl chloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04251262 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-d23cd4887ff7408983a0b0e4c727b1e3 |
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| Source note | uspto-grants-1981_02 |
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