Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1-(2,6-Difluoropyridin-3-yl)ethanone | HCID 25132244 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178434471 | HCID 178434471 | — |
Reaction Steps
To a stirred solution of 7.46 g (47.51 mmol) of 1-(2,6-difluoropyridin-3-yl)ethanone (37-2) in 50 mL of CH2Cl2 under nitrogen was added dropwise titanium (IV) isopropoxide. The resulting solution was stirred vigorously for 15 minutes before hydrazine hydrate (4.62 g, 95.0 mmol) was added slowly to form a thick slurry. The reaction mixture was stirred for 1 hour before the addition of 11 mL of H2O, and the resulting mixture stirred for 1.5 hours until completion as determined by LC/MS analysis. The solid matter was filtered off and the filterate was condensed to yield a white solid. EtOH (100 mL) was added to the crude intermediate and the mixture was heated to reflux for 6 hours. After the reaction was complete as determined by LC/MS analysis the solvent was removed to yield the desired product. No further purification was necessary. 1H NMR (CDCl3): 2.56 (s, 3H), 6.78 (d, 1H), 8.08 (t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807684B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-1b8b409aeb5b4d4cb1e1372695165ba1 |
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| Source note | uspto-grants-2010_10 |
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