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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746264Generated: October 23, 2026

4-Hydroxy-2,2,6,6-tetramethylpiperidine → 2,2,6,6-Tetramethylpiperidin-4-yl 2,5-dimethylfuran-3-carboxylate

https://huagongshe.com/en/reaction/746264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-2,2,6,6-tetramethylpiperidineHCID 75471—
Reactant3-Furancarboxylic acid, 2,5-dimethyl-, methyl esterHCID 80248—
CatalystTetrabutoxytitaniumHCID 521701—
SolventMethanolHCID 887—
Product2,2,6,6-Tetramethylpiperidin-4-yl 2,5-dimethylfuran-3-carboxylateHCID 13765634—

Reaction Steps

154 g (1 mole) of methyl 2,5-dimethylfuran-3-carboxylate and 157 g (1 mole) of 4-hydroxy-2,2,6,6-tetramethylpiperidine were heated together with 10 g of tetrabutyl orthotitanate for 10 hours at about 190° C., the methanol formed being distilled off. When the reaction is complete, the mixture is cooled and the reaction mass is dissolved in ethyl acetate. The solution is extracted by shaking, first with 10% strength sodium carbonate solution and then with water, after which it is dried and evaporated down, and the residue is distilled under reduced pressure. The desired product distils at 142° C./2 mm as a virtually colorless oil which soon solidifies to a solid of melting point 59°-61° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04603205
Source datasetuspto-grants-1986_07
ORD IDord-66b19aa7576741619657092ed9d7f36e
Source noteuspto-grants-1986_07