HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852078Generated: October 30, 2026
Pyridine → (2,4-Difluoro-phenyl)-(3-methoxy-phenyl)-methanone oxime
https://huagongshe.com/reaction/852078
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | (2,4-Difluorophenyl)(3-methoxyphenyl)methanone | HCID 17906337 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | (2,4-Difluoro-phenyl)-(3-methoxy-phenyl)-methanone oxime | HCID 72465824 | 99% |
Reaction Steps
Combine (2,4-difluoro-phenyl)-(3-methoxy-phenyl)-methanone (51.2 g, 0.206 mol) and pyridine (293.4 g, 300 mL). Add hydroxylamine hydrochloride (21.7 g, 0.312 mol) and heat to 100° C., under a nitrogen atmosphere, for 4 hours. TLC (20% ethyl acetate in heptane) shows that the reaction is complete. Concentrate the reaction mixture and dry (vacuum at 50° C.). Distribute the material between ethyl acetate and water. Wash the organic layer with 10% HCl, saturated sodium chloride, dry (MgSO4) and concentrated to obtain the title compound as a white solid (53.66 g, 99% Yield). Use compound in a crude form or recrystallize from heptane and dry (P2O5). NMR and MS are consistent with the final, desired compound, which is a mixture of the Z-isomer (81%) and the E-isomer (19%). mp=122° C.-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253165B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-29c3e4da9edd4a1bba5d4c9a6b16122d |
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| Source note | uspto-grants-2007_08 |
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