HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Fluoropyridine → HCID 18321141, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Fluoropyridine | HCID 67794 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | Cyclohexane diethylether | HCID 21895417 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18321141 | HCID 18321141 | — |
Reaction Steps
To a solution of 5.0 g (0.0515 mol) of 3-fluoropyridine and 43.5 ml of 1-(phenylmethyl)piperazine in 300 ml of anhydrous diethylether was added dropwise, at boiling temperature, within 2.5 hours, 56 ml (0.112 mol) of a 2 molar solution of phenyl-lithium in a cyclohexane-diethylether mixture (7/3 v/v) and the resulting mixture was then kept at reflux temperature for a further 4 hours. The crude reaction product obtained as an oil after working up in the usual way was purified by column chromatography over silica gel (30-60 μm) using FM1/cyclohexane (7/3 v/v) as eluant. 12.0 g (92% of theory) of a colourless oil were obtained, Rf 0.52 (FM4; Macherey-Nagel, POLYGRAM® SIL G/UV254 Pre-coated plastic sheets for TLC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07498325B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-bc115b73d8254c46b155ef5962d23ab0 |
| Source note | uspto-grants-2009_03 |