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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 496833Erstellt: 24. Oktober 2026

Dichloromethane → 1,3-dimethoxycarbonyl-O-methylisourea

https://huagongshe.com/de/reaction/496833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktMethyl chloroformateHCID 6586—
EduktSodium CarbonateHCID 10340—
EduktSodium HydroxideHCID 14798—
EduktCarbamimidic acid, methyl ester, sulfate (1:1)HCID 169039—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
Produkt1,3-dimethoxycarbonyl-O-methylisoureaHCID 85348789—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06946554B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-85697c4cfef349d48d942fc9e44a1f8b
Quellennotizuspto-grants-2005_09