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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039694Generated: November 1, 2026

Acetaldehyde → 1-(3-(Methoxymethoxy)pyridin-4-yl)ethanol

https://huagongshe.com/reaction/1039694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
Reactant3-(Methoxymethoxy)pyridineHCID 3754397—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product1-(3-(Methoxymethoxy)pyridin-4-yl)ethanolHCID 5751585136%

Reaction Steps

A solution of 3-(methoxymethoxy)pyridine (9.8 g, 70 mmol) and THF (40 mL) was added to a stirring mixture of tert-butyllithium (91 mL of a 1.7 M solution with pentane, 160 mmol) and THF (100 mL) at −78° C. After 1 h, acetaldehyde (9.9 mL, 180 mmol) was added, and the reaction mixture was stirred for 3 h and then warmed to RT. After 21 h, the reaction mixture was partitioned between ethyl acetate and saturated aqueous NaHCO3, the layers were separated, the organic material was washed with saturated aqueous NaHCO3, brine, dried (Na2SO4), filtered, and the filtrate was concentrated. The residue was purified by flash chromatography on silica gel (1:1 hexane-ethyl acetate) to afford 4.6 g (36%) of 1-(3-(methoxymethoxy)pyridin-4-yl)ethanol as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552181B2
Source datasetuspto-grants-2013_10
ORD IDord-fb0d6b725eeb4395809b5b1b3c475a66
Source noteuspto-grants-2013_10