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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1164467생성일: 2026년 10월 27일

Urea → Ethyl N-(aminocarbonyl)carbamate

https://huagongshe.com/reaction/1164467

반응식

참여 물질

역할이름HCID투입량
반응물UreaHCID 1176—
반응물Ethoxycarbonyl carbonateHCID 86738757—
용매ChloroformHCID 6212—
생성물Ethyl N-(aminocarbonyl)carbamateHCID 69380—

반응 단계

0.65 ml (0.72 g, 0.00443 moles) of ethyl pyrocarbonate are added to a solution of 1.0 g (0.00285 moles) of 1-(1',3'-bis/2",6"-dimethylphenyl/-4'-methyl-imidazolidine-2'-ylidene)-urea, prepared as described in Example 72, in 10 ml of dry chloroform, and the mixture is allowed to stand at room temperature for 48 hours. Thereafter the solvent and the excess of the reactant are distilled off under reduced pressure. The oily residue is dissolved in 10 ml of diethyl ether, the insolubles are filtered off, and the filtrate is concentrated to a final volume of about 2 ml. Next day the separated crystalline product is filtered off, washed with a small amount of diethyl ether and dried. 0.5 g (41.7%) of 1-(1',3'-bis/2",6"-dimethylphenyl/-4'-methyl-imidazolidine-2'-ylidene)-3-carbethoxy-urea are obtained; m.p.: 123°-125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04369325
출처 데이터셋uspto-grants-1983_01
ORD IDord-7a34ac528a9d4747be3a1a2afc67091f
출처 메모uspto-grants-1983_01