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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4228Erstellt: 23. Oktober 2026

Citric Acid → N-[2-(Diethylamino)ethyl]-N-methyl-N'-(1-methylethyl)-N'-[2-(phenylsulfonyl)ethyl]urea citrate hydrate

https://huagongshe.com/de/reaction/4228

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
EduktTriethylamineHCID 8471—
Edukt1,2-Ethanediamine, N1,N1-diethyl-N2-methyl-HCID 66034—
EduktN-(1-methylethyl)-N-[2-(phenylsulfonyl)ethyl]carbamic chlorideHCID 13655164—
LösungsmittelMethanolHCID 887—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-[2-(Diethylamino)ethyl]-N-methyl-N'-(1-methylethyl)-N'-[2-(phenylsulfonyl)ethyl]urea citrate hydrateHCID 70419038—

Reaktionsschritte

A mixture of 6.65 g (0.023 mole) of N-(1-methylethyl)-N-[2-(phenylsulfonyl)ethyl]carbamic chloride; 3.0 g (0.023 mole) of N,N-diethyl-N'-methylethylenediamine and triethylamine (2.7 g, 0.0267 mole) in 400 ml of tetrahydrofuran was stirred at room temperature for 10 hr. The solvent was removed in vacuo, and the residue was dissolved in a 60/40 mixture of ether and methylene chloride. This solution was extracted with several portions of water and was dried over magnesium sulfate. The solvent was removed in vacuo to give an oil. This was dissolved in methanol, an excess of citric acid was added, and ether was added. A solid precipitated to give 11.08 g (82.4%) of white, crystalline solid; m.p. 77°-82° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04724235
Quelldatensatzuspto-grants-1988_02
ORD IDord-1bbdfdf4f42246edb2dbfdf161a6a0b2
Quellennotizuspto-grants-1988_02