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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638586Generated: October 31, 2026

(4-methoxypyridin-2-yl)methyl Acetate → (4-Methoxy-pyridin-2-yl)-methanol

https://huagongshe.com/reaction/638586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-methoxypyridin-2-yl)methyl AcetateHCID 10726082—
CatalystMercuryHCID 23931—
SolventHydrochloric AcidHCID 313—
Product(4-Methoxy-pyridin-2-yl)-methanolHCID 1082059667%

Reaction Steps

A solution of 2-acetoxymethyl-4-methoxypyridine (20.72 g, 0.114 mole) in 3M hydrochloric acid (100 ml) was heated under reflux for 1 hour. The resulting solution was concentrated under reduced pressure and the residue neutralised by addition of potassium carbonate. The mixture was extracted with dichloromethane and the organic solution dried over anhydrous sodium sulphate, filtered and evaporated to give a light coloured viscous oil which solidified on standing to yield the title compound (10.6 g, 67%) b.p. 135° C. at 0.1 mm mercury.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562197
Source datasetuspto-grants-1985_12
ORD IDord-d43c60e54378460d8ad0d58a360d0b13
Source noteuspto-grants-1985_12