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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407479Generated: October 31, 2026

4-(Trifluoromethyl)benzoic acid → HCID 59509432, compound

https://huagongshe.com/reaction/2407479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoic acidHCID 9966—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 178513316HCID 178513316—
SolventDimethylformamideHCID 6228—
ProductHCID 59509432HCID 59509432—

Reaction Steps

A mixture of 4-trifluoromethylbenzoic acid (6 g, 0.032 mol), 1-(3-dimethylaminopropyl)-3-ethyl-carbodiimide (6.05 g, 0.0315 mol) and 1-hydroxy-benzotriazole hydrate (4.82 g, 0.032 mol) in N,N-dimethylformamide (30 mL) is stirred at room temperature for 30 minutes. N-Hydroxy-4-hydroxymethylbenzamidine (6.97 g, 90%, 0.038 mol) is added and the reaction mixture is heated at reflux for 3 hrs, then allowed to come to room temperature and solvent is removed under reduced pressure. An aqueous solution (100 mL) of sodium bicarbonate is added to the residue and the aqueous layer is extracted with ethyl acetate (2×100 mL). Combined organic layers are dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue is purified by column chromatography (silica gel 230-400 mesh, n-hexane:ethyl acetate, 65:35) to give 4-[5-(4-trifluoromethylphenyl)-1,2,4-oxadiazol-3-yl]phenylmethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809539B2
Source datasetuspto-grants-2014_08
ORD IDord-95a3d25684ad4fe6a9af7db3b48b0426
Source noteuspto-grants-2014_08