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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654342Erstellt: 26. Oktober 2026

Triethylamine → 5-(4'-Ethoxycarbonyloxy-3'methoxyphenyl)pentadienoic acid geranylamide

https://huagongshe.com/reaction/654342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl chloroformateHCID 10928—
Edukt5-(4-Hydroxy-3-methoxyphenyl)penta-2,4-dienoic acidHCID 54216809—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-(4'-Ethoxycarbonyloxy-3'methoxyphenyl)pentadienoic acid geranylamideHCID 86745990—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

Separately, 2.33 g of 5-(4'-hydroxy-3'-methoxyphenyl)pentadienoic acid is suspended in 50 ml of methylene chloride under an argon atmosphere. To the suspension cooled to -10° C. are added 2.95 ml of triethylamine and 2.03 ml of ethyl chlorocarbonate. To the mixture, after stirred for 30 min., is added a suspension of the geranylamine-hydrazide mixture in methylene chloride. The resulting mixture is stirred at -10° C. to 0° C. for 4 hours. The reaction mixture is filtered, and precipitates are washed with methylene chloride. Combined filtrate and washing are washed successively with water and saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The solvent is distilled off under reduced pressure, and the residue is subjected to column chromatography on silica gel. From the fraction eluted with chloroform is obtained 2.61 g of 5-(4'-ethoxycarbonyloxy-3'methoxyphenyl)pentadienoic acid geranylamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05130483
Quelldatensatzuspto-grants-1992_07
ORD IDord-210e7e0b83344971938b661da57056c9
Quellennotizuspto-grants-1992_07