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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387513Generated: October 28, 2026

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

https://huagongshe.com/reaction/2387513

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 at 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 (19 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), 7.88-7.81 (dt, 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), 5.96-5.95 (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 numberUS08268868B2
Source datasetuspto-grants-2012_09
ORD IDord-16b592ba04a34150aa9eac22ba0e3ebf
Source noteuspto-grants-2012_09