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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761400Generated: November 1, 2026

2-Methyl-4-methoxypyridine-N-oxide → (4-methoxypyridin-2-yl)methyl Acetate

https://huagongshe.com/reaction/1761400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-methoxypyridine-N-oxideHCID 10701893—
Reactant2-Acetoxymethyl-6-chloropyridineHCID 10726190—
Product(4-methoxypyridin-2-yl)methyl AcetateHCID 10726082—

Reaction Steps

Starting with 2-methyl-4-methoxypyridine-1-oxide (2.1 g) in the procedure of Part (ii) afforded 2.5 g of 2-acetoxymethyl-4-methoxypyridine which was contaminated with about 25% of 5-acetoxy-2-methyl-4-methoxypyridine. This mixture was dissolved in methanol (10 ml) containing 1.118 g (20.7 mmole) sodium methoxide and stirred at reflux for one hour. The methanol was evaporated in vacuo, the residue diluted with water, neutralized with dilute hydrochloric acid, and extracted with chloroform. The organic layer was washed with brine, dried (MgSO4) and concentrated in vacuo to give 853 mg (41%) 2-hydroxymethyl-4-methoxypyridine. 1H--NMR(CDCl3)ppm (delta): 3.9 (s, 3H), 4.72 (s, 2H), 5.35 (bs, 1H), 6.7 (dd, 1H), 6.95 (d, 1H), 8.3 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826833
Source datasetuspto-grants-1989_05
ORD IDord-a58f96cf2a5046a0840ba76c76158a47
Source noteuspto-grants-1989_05