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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032108Generated: October 27, 2026

Triethylamine → N-(2-Methyl-2-propenyl)-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide

https://huagongshe.com/reaction/1032108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-MethylallylamineHCID 76141—
Reactant3-[4-(Trifluoromethyl)phenoxy]azetidine oxalateHCID 12812500—
SolventDichloromethaneHCID 6344—
ProductN-(2-Methyl-2-propenyl)-3-[4-(trifluoromethyl)phenoxy]-1-azetidinecarboxamideHCID 1505342658.9%

Reaction Steps

A stirred solution of 3.6 g (0.022 mole) of 1,1'-carbonyldiimidazole in 75 ml of methylene chloride under nitrogen was treated with 1.6 g (0.022 mole) of 2-methyl-2-propenylamine (added via a syringe and needle through a septum placed in one neck of the reaction flask). After stirring for 1 hr, 6.2 g (0.02 mole) of 3-[4-(trifluoromethyl)phenoxy]azetidine oxalate was added all at once followed in 30 min with 5 ml of triethylamine and stirring was continued for 3 hr. The reaction mixture was washed with water (2×25 ml), dried over magnesium sulfate and concentrated in vacuo. The oily residue solidified on standing and was recrystallized from isopropyl ether to yield 3.7 g (58.9%) of fine white crystals, m.p. 101°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956359
Source datasetuspto-grants-1990_09
ORD IDord-93bf0e18cdb343bb8c375ded96a8d646
Source noteuspto-grants-1990_09