Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5011Erstellt: 23. Oktober 2026

Nicotinic Acid → Nicotinoyl chloride

https://huagongshe.com/de/reaction/5011

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNicotinic AcidHCID 938—
EduktThionyl ChlorideHCID 24386—
Edukt4-(4-Tert-butylphenoxy)butan-1-OLHCID 13313737—
LösungsmittelDichloromethaneHCID 6344—
ProduktNicotinoyl chlorideHCID 82604—

Reaktionsschritte

Nicotinoyl chloride was prepared by treating 100 g (0.81 mole) of nicotinic acid with 280 ml of thionyl chloride at reflux for two hours. The excess thionyl chloride was removed in vacuo and the crystalline acid chloride hydrochloride was suspended in 500 ml of dichloromethane. To the stirred mixture was added 66 g (0.30 mole) of 4-p-t-butylphenoxy-1-butanol dissolved in 400 ml of dichloromethane. After forty-eight hours the mixture was washed with one liter of saturated sodium bicarbonate. The dichloromethane solution was dried over magnesium sulfate and evaporated to a syrupy residue. The material was chromatographed on 1 kg of silica gel with elution by dichloromethane-methanol, 96:4, to afford 43.8 g (45%) of the nicotinate ester as an oil. The hydrobromide salt was prepared by treatment of a solution of 43.8 g in 800 ml of ethyl acetate with 30 ml of 4.5N hydrogen bromide in ether. The precipitate was collected, washed with pentane and dried, m.p. 132°-133° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05242936
Quelldatensatzuspto-grants-1993_09
ORD IDord-d238f04b14bc48fe99e1c99449a0250c
Quellennotizuspto-grants-1993_09