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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413755Generated: November 1, 2026

Tetrahydrofuran → [3,5-Bis(dimethylamino)-4-(piperidin-1-yl)phenyl]methanol

https://huagongshe.com/reaction/1413755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 3,5-bis(dimethylamino)-4-(piperidin-1-yl)benzoateHCID 20290445—
ReactantAluminium lithium hydrideHCID 21226445—
SolventEthyl AcetateHCID 8857—
Product[3,5-Bis(dimethylamino)-4-(piperidin-1-yl)phenyl]methanolHCID 53863713—

Reaction Steps

A solution of 25 g. of methyl 3,5-bis(dimethylamino)-4-piperidinobenzoate in 150 ml. of absolute tetrahydrofuran was added dropwise to a solution of lithium aluminum hydride in 300 ml. of absolute tetrahydrofuran, and the mixture was boiled under reflux for 3 hours. After cooling, the excess lithium aluminum hydride was cautiously decomposed with 100 ml. of ethyl acetate and then with 3 ml. of water and the solution evaporated to dryness. The residue was taken up in water, the oily product extracted with ethyl acetate and the ethyl acetate solution dried and evaporated. After recrystallization from high-boiling petroleum ether, there was obtained 3,5-bis(dimethylamino)-4-piperidinobenzyl alcohol having a melting point of 90°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251454
Source datasetuspto-grants-1981_02
ORD IDord-4dda835078ed4545a1d88cbe90a82f2e
Source noteuspto-grants-1981_02