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
Participants
| Role | Name | HCID | Charge |
|---|
| 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268868B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-16b592ba04a34150aa9eac22ba0e3ebf |
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| Source note | uspto-grants-2012_09 |
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