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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26712생성일: 2026년 10월 24일

Diethylcarbamoyl chloride → N,N-dimethyl-2-[(diethylcarbamoyl)oxyimino]-3-methoxyiminobutyramide

https://huagongshe.com/ko/reaction/26712

반응식

참여 물질

역할이름HCID투입량
반응물Diethylcarbamoyl chlorideHCID 6916—
반응물Sodium hydrideHCID 24758—
반응물N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramideHCID 136099002—
반응물HCID 178418361HCID 178418361—
용매TetrahydrofuranHCID 8028—
생성물N,N-dimethyl-2-[(diethylcarbamoyl)oxyimino]-3-methoxyiminobutyramideHCID 54436333—

반응 단계

To a stirred mixture of 75 parts of N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramide and 1500 parts of tetrahydrofuran was added portionwise over a fifteen-minute period 19 parts of 50% sodium hydride, mineral oil dispersion. The temperature was maintained in the range of 20° C. to 30° C. After about one-half hour, evolution of hydrogen gas ceased, and rapid addition of 55 parts diethylcarbamoyl chloride was begun. The temperature spontaneously rose to 33° C., and rapid thinning-out of the oxime salt slurry occurred. The mixture was refluxed and stirred for three hours. The inorganic solids were then removed by filtration and the product recovered by removal of the solvent under reduced pressure. The residue was twice triturated with hexane and the liquid decanted to remove the mineral oil. After drying, there was obtained 90 parts of N,N-dimethyl-2-[(diethylcarbamoyl)oxyimino]-3-methoxyiminobutyramide, m.p. 59°-61°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04151296
출처 데이터셋uspto-grants-1979_04
ORD IDord-a523c9ba4d524ffdbd3c37d2785780ee
출처 메모uspto-grants-1979_04