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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081432Generated: October 26, 2026

Isobutylamine → N-(2-Methylpropyl)-3-[4-(trifluoromethyl)phenoxy]-1 azetidinecarboxamide

https://huagongshe.com/reaction/2081432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutylamineHCID 6558—
ReactantTriethylamineHCID 8471—
Reactant3-[4-(Trifluoromethyl)phenoxy]azetidine oxalateHCID 12812500—
SolventDichloromethaneHCID 6344—
ProductN-(2-Methylpropyl)-3-[4-(trifluoromethyl)phenoxy]-1 azetidinecarboxamideHCID 1979961085.4%

Reaction Steps

A stirred solution of 3.6 g (0.022 mole) of 1,1-carbonyldiimidazole in 100 ml of methylene chloride under nitrogen was treated with 1.6 g (0.022 mole) of 2-methylpropylamine (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 18 hr. The reaction mixture was washed with water (2×25 ml), dried over magnesium sulfate, and concentrated in vacuo. The solid residue was recrystallized from ethanol/water, yielding 5.4 g (85.4%) of pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183902
Source datasetuspto-grants-1993_02
ORD IDord-46b9ef6f4e8c40a7b218aefbac574edc
Source noteuspto-grants-1993_02