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HRID 26712作成日:2026年10月25日

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

https://huagongshe.com/reaction/26712

反応式

関与物質

役割名称HCID仕込み量
反応物Diethylcarbamoyl chlorideHCID 6916—
反応物Sodium hydrideHCID 24758—
反応物N,N-dimethyl-2-hydroxyimino-3-methoxyiminobutyramideHCID 136099002—
反応物HCID 178418361HCID 178418361—
溶媒TetrahydrofuranHCID 8028—
生成物N,N-dimethyl-2-[(diethylcarbamoyl)oxyimino]-3-methoxyiminobutyramideHCID 54436333—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04151296
出典データセットuspto-grants-1979_04
ORD IDord-a523c9ba4d524ffdbd3c37d2785780ee
出典メモuspto-grants-1979_04