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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 974644Erstellt: 25. Oktober 2026

Ammonia → Dezinamide

https://huagongshe.com/reaction/974644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktPhosgeneHCID 6371—
EduktChlorodiphenylmethaneHCID 7035—
EduktPotassium CarbonateHCID 11430—
Edukt1-Benzhydryl-3-[3-(trifluoromethyl)phenoxy]azetidineHCID 11728694—
Edukt1-Chlorocarbonyl-3-[3-(trifluoromethyl)phenoxy]azetidineHCID 19799606—
LösungsmittelTolueneHCID 1140—
ProduktDezinamideHCID 146291—

Reaktionsschritte

A 16 ml solution containing 5.94 g of phosgene was prepared by dissolving phosgene gas in cold toluene. This solution was stirred with 7 g potassium carbonate in an acetone-ice bath for about 10 minutes. To this solution in the bath was added dropwise over a 13 minute period at -9° C. to +4° C. a solution of 19.2 g (0.050 mole) of 1-(diphenylmethyl)-3-[3-(trifluoromethyl)phenoxy]azetidine in 38.4 ml of toluene. The cold bath was removed and the temperature of the reaction mixture rose to 18° C. after 1/2 hr. TLC (silica gel eluted with methylene chloride) of a sample indicated all the 1-(diphenylmethyl)-3-[3-(trifluoromethyl)phenoxy]azetidine had disappeared (reacted). After 1 hr, the mixture was filtered to remove solid, leaving a filtrate containing 3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarbonyl chloride and diphenylchloromethane. The filtrate was added (over a 7 min period) to about 30 ml of liquid ammonia at - 60° to -30° C. Some white solid formed in the mixture. The ammonia was refluxed under a dry ice-acetone condenser for 1/2 hr and then allowed to evaporate using nitrogen gas to facilitate the removal of ammonia. Petroleum ether (60 ml) was added to the mixture and the resulting white solid was collected by filtration and rinsed twice with petroleum ether to give 18.1 g of solid. The solid was stirred in 90 ml of water at room temperature for one hr, filtered off, rinsed twice with water and dried under vacuum at about 60° C. for 2 hr to give 13 g (100%) of title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05068231
Quelldatensatzuspto-grants-1991_11
ORD IDord-d892c5c016a1416e81ab8a1a2a1673e9
Quellennotizuspto-grants-1991_11