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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020560Generated: October 27, 2026

Acetic Anhydride → 4-(Pyridin-2-ylmethoxy)pyridin-2(1H)-one

https://huagongshe.com/reaction/1020560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-(Pyridin-2-ylmethoxy)pyridine 1-oxideHCID 68458440—
Product4-(Pyridin-2-ylmethoxy)pyridin-2(1H)-oneHCID 5795028321%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(Pyridin-2-ylmethoxy)pyridine 1-oxide (9.0 g, 45 mmol) was heated to 140° C. in acetic anhydride (100 mL) for 2 h. The solution was concentrated and then heated at 80° C. for 1 h in a mixture of MeOH (50 mL) and H2O (50 mL). The resultant black solution was concentrated and the residue was dissolved in hot i-PrOH (40 ml). Et2O (250 mL) was added and the mixture was placed in the freezer for 16 h. The solid was filtered off to provide the title compound (1.9 g, 21%) as a brown solid: 1H NMR (300 MHz, DMSO-d6) δ 11.13 (br s, 1H), 8.58 (d, J=4.7 Hz, 1H), 7.85 (overlapping ddd, J=7.9, 1.6 Hz, 1H), 7.49 (d, J=7.9 Hz, 1H), 7.38-7.34 (m, 1H), 7.26 (d, J=7.3 Hz, 1H), 5.96 (dd, J=7.3, 2.5 Hz, 1H), 5.76 (d, J=3.4 Hz, 1H), 5.12 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716308B2
Source datasetuspto-grants-2014_05
ORD IDord-b2e6f184cdc1431fa9dc51028ec9c3f0
Source noteuspto-grants-2014_05