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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1769263Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → 2-Allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetate

https://huagongshe.com/de/reaction/1769263

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt3-Pyridinamine, N,N-dimethyl-HCID 123378—
Edukt2-Propanol, 1-(2-propenyloxy)-HCID 542178—
EduktCloquintocetHCID 15257197—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetateHCID 1548412972,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

5.0 g (0.021 mol) of 5-chloroquinolin-8-oxyacetic acid and 2.44 g (0.021 mol) of 2-allyloxy-1-methylethanol are suspended in a mixture of 40 ml of methylene chloride and 40 ml of dimethylformamide and the suspension is cooled to 0° C. 4.78 g (0.023 mol) of dicyclohexylcarbodiimide, dissolved in 10 ml of methylene chloride, are added dropwise at this temperature, and 200 mg of 3-(N,N-dimethylamino)-pyridine are then added. The mixture is stirred at room temperature for 15 hours and the precipitate which has separated out is filtered off with suction and rinsed with 50 ml of methylene chloride. The filtrate is washed with 100 ml of 0.5 N HCl, with 100 ml of potassium bicarbonate solution and with 3 portions of in each case 50 ml of water. The organic phase is dried over magnesium sulfate and the solvent is stripped off in vacuo. The residue is recrystallized from n-heptane. 5.1 g (72.4% of theory) of 2-allyloxy-1-methylethyl 5-chloroquinolin-8-oxyacetate of melting point 59° C. are obtained in this manner.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05380852
Quelldatensatzuspto-grants-1995_01
ORD IDord-df1b135afad3466692a98882f3761cf4
Quellennotizuspto-grants-1995_01