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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 721200Erstellt: 24. Oktober 2026

3-Hexanol → 1-Ethylbutyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}carbamate

https://huagongshe.com/de/reaction/721200

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-HexanolHCID 12178—
EduktTriphosgeneHCID 94429—
EduktSodium BicarbonateHCID 516892—
Edukt4-[(6,7-Dimethoxyquinolin-4-yl)oxy]anilineHCID 11594543—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produkt1-Ethylbutyl N-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}carbamateHCID 2189082090,7%

Reaktionsschritte

4-[(6,7-Dimethoxy-4-quinolyl)oxy]aniline (100 mg) was added to toluene (10 ml) and triethylamine (1 ml), and the mixture was heated under reflux to prepare a solution. A solution of triphosgene (151 mg) in methylene chloride was then added thereto, and the mixture was heated under reflux for 10 min. Next, 3-hexanol (52 mg) was added thereto, and the mixture was further stirred with heating under reflux for 3 hr. A saturated aqueous sodium bicarbonate solution was added to stop the reaction, and the reaction solution was then extracted with chloroform, followed by washing with a 1 N aqueous hydrochloric acid solution, water, and saturated brine in that order. The extract was dried over sodium sulfate and was then concentrated. The residue was purified on a column using chloroform/methanol to give the title compound (130 mg, yield 83%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135466B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-56e4c295f44c46558e33d7b19257bac0
Quellennotizuspto-grants-2006_11