HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[4-[(E)-C-(2,4-dichlorophenyl)-N-hydroxycarbonimidoyl]piperidin-1-yl]ethanone → HCID 66741568, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[4-[(E)-C-(2,4-dichlorophenyl)-N-hydroxycarbonimidoyl]piperidin-1-yl]ethanone | HCID 13076404 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66741568 | HCID 66741568 | 75% |
Reaction Steps
1-(4-{(2,4-Dichloro-phenyl)-[(E)-hydroxyimino]-methyl}-piperidin-1-yl)-ethanone (2.15 g, 7 mmol) was solved in THF (34 mL) and potassium tert-butoxide was added (0.844 g, 7.5 mmol). The mixture was stirred for 2 hours until TLC indicated the end of the reaction. The solvent was removed and the mixture purified by flash-chromatography on silica gel with hexane:ethyl acetate (1:0 to 0:1). The combined producted fractions were evaporated under reduced pressure to yield 1.45 g of a colourless oil (75%). MS (m/e): 279.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829029B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-4e66d41e08544725ac1cf4a983bae41f |
| Source note | uspto-grants-2014_09 |