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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081442Generated: October 26, 2026

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

https://huagongshe.com/reaction/2081442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant3-(4-Fluorophenoxy)-1-azetidinecarbonyl chlorideHCID 15053367—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Fluorophenoxy)-N-methyl-1-azetidinecarboxamideHCID 15053437129.3%

Reaction Steps

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 with 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183902
Source datasetuspto-grants-1993_02
ORD IDord-06377ae048764de4a9b4755fb96012d2
Source noteuspto-grants-1993_02