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HRID 496833作成日:2026年10月26日

Dichloromethane → 1,3-dimethoxycarbonyl-O-methylisourea

https://huagongshe.com/reaction/496833

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Methyl chloroformateHCID 6586—
反応物Sodium CarbonateHCID 10340—
反応物Sodium HydroxideHCID 14798—
反応物Carbamimidic acid, methyl ester, sulfate (1:1)HCID 169039—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒WaterHCID 962—
生成物1,3-dimethoxycarbonyl-O-methylisoureaHCID 85348789—

反応手順

A three-neck flask fitted with a mechanical stirrer was charged with H2O (1.1 L), CH2Cl2 (1 L) and Na2CO3 (254.4 g, 2.4 mol) and the mixture chilled to ca 5° C. To the chilled mixture was then added the O-methylisourea hydrogen sulfate from above, tetrabutylammonium bromide (0.5 g) and methyl chloroformate (556 mL, 7.2 mol). The mixture was stirred vigorously and 25% NaOH (144 g in ca. 600 mL) was added over 0.5 h. After the last addition, the mixture was stirred for an additional 2 h and then filtered through Celite to remove inorganic salts (Na2SO4). The layers were separated and the organic layer dried (Na2SO4), filtered and concentrated to give the title compound as a thick syrup. The syrup was dried in vacuo overnight during which time it solidified to give 114.7 g (0.6 mol. 53%) of 1,3-dimethoxycarbonyl-O-methylisourea.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06946554B2
出典データセットuspto-grants-2005_09
ORD IDord-85697c4cfef349d48d942fc9e44a1f8b
出典メモuspto-grants-2005_09