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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112720Generated: November 3, 2026

Hydrochloric Acid → 3-Pyridinol, 4-(aminomethyl)-6-(1,1-dimethylethyl)-, hydrochloride (1:2)

https://huagongshe.com/reaction/1112720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(1,1-Dimethylethyl)-5-hydroxy-4-pyridinecarbonitrileHCID 12634260—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-Pyridinol, 4-(aminomethyl)-6-(1,1-dimethylethyl)-, hydrochloride (1:2)HCID 12634262—

Reaction Steps

A solution of 4-cyano-6-(1,1-dimethylethyl)-3-pyridinol (5.7 g., 0.032 mole) in methanol -- 12N hydrochloric acid (30:1; v:v; 310 ml.) is hydrogenated in the presence of 10% palladium on charcoal (1 g.) in a Parr apparatus at 25° C. and 40-45 p.s.i. pressure until the theoretical quantity of hydrogen has been consumed. Then the hydrogenation mixture is filtered and the collected catalyst, washed with ethanol. Evaporation (in vacuo) of the combined filtrate and washings leaves the 4-aminomethyl-6-(1,1-dimethylethyl)-3-pyridinol dihydrochloride as a residual solid (7.9 g., 98%), m.p. 304°-306° C. with dec. Recrystallization of the solid from ethanol-ether-water (100:100:4; v:v:v) affords an analytical sample of 4-aminomethyl-6-(1,1-dimethylethyl)-3-pyridinol dihydrochloride as colorless crystals, m.p. 304°-306° C. with dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123537
Source datasetuspto-grants-1978_10
ORD IDord-215c1bcd324e4b4fb2acf26cf37ae888
Source noteuspto-grants-1978_10