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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(Pyridin-2-ylmethoxy)pyridine 1-oxide | HCID 68458440 | — |
| Product | 4-(Pyridin-2-ylmethoxy)pyridin-2(1H)-one | HCID 57950283 | 21% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716308B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-b2e6f184cdc1431fa9dc51028ec9c3f0 |
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| Source note | uspto-grants-2014_05 |
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