HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | p-Bromophenyl octyl ether | HCID 145298 | — |
| Reactant | 2-Fluoro-6-octyloxypyridine-3-boronic acid | HCID 19046940 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridine | HCID 19046969 | 41.5% |
Reaction Steps
2.00 g (7.44 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid, 1.64 g (5.72 mmol) of 1-bromo-4-octyloxybenzene, 0.26 g (0.22 mmol) of tetrakis(triphenylphosphine)palladium(0) and 11.16 ml (22.32 mmol) of 2-molar sodium carbonate solution are refluxed in 20 ml of benzene and 10 ml of ethanol for 6 hours. After distributing the reaction mixture between water and diethyl ether, the organic phase is washed with water, dried over sodium sulfate, filtered and concentrated. Purification of the residue by chromatography (silica gel, 95:5 hexane/ethyl acetate) and recrystallization from acetonitrile give 1.02 g of 2-fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridine. ##STR23##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05630962 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-dbb292851d0f40bdbc3c5e9e4eedc4a7 |
| Source note | uspto-grants-1997_05 |