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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 974603Erstellt: 26. Oktober 2026

Methylamine → 3-(4-Fluorophenoxy)-N-methyl-1-azetidinecarboxamide

https://huagongshe.com/reaction/974603

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
Edukt3-(4-Fluorophenoxy)-1-azetidinecarbonyl chlorideHCID 15053367—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(4-Fluorophenoxy)-N-methyl-1-azetidinecarboxamideHCID 15053437129,3%

Reaktionsschritte

A solution of 4.6 g (0.02 mole) of 3-(4-fluorophenoxy)-1-azetidinecarbonyl chloride in 15 ml of tetrahydrofuran was stirred while 6.2 g (0.08 mole) of 40% aqueous methylamine was added. The reaction mixture was exothermic and was allowed to cool to ambient temperature while stirring for 18 hr. The reaction mixture was diluted with 200 ml of ice water and the oil droplets which separated quickly crystallized. Filtration yielded 6.6 g of crude product. The solid was dissolved in 100 ml of methylene chloride, treated with 15 g of silica gel and stirred for 2 hr. The silica gel was removed by filtration and washed wit 200 ml of 50/50 ethyl acetatemethylene chloride. The combined filtrates were concentrated on a rotary evaporator, yielding 5.8 g of solid residue. The solid was recrystallized by dissolving in 22 ml of acetone and adding 88 ml of isopropyl ether. The volume was reduced to 40 ml by boiling under nitrogen atmosphere and upon cooling the product crystallized. Filtration yielded 2.95 (66.7%) of white crystals, m.p. 140°-142° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05068231
Quelldatensatzuspto-grants-1991_11
ORD IDord-f75f0d7ea04c43aaa84e1e4db2741c27
Quellennotizuspto-grants-1991_11