HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloropyridine → 2-(2-{4-[(Butan-2-yl)oxy]phenoxy}propoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloropyridine | HCID 7977 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-{4-[(Butan-2-yl)oxy]phenoxy}propan-1-ol | HCID 15662578 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 2-(2-{4-[(Butan-2-yl)oxy]phenoxy}propoxy)pyridine | HCID 15239094 | — |
Reaction Steps
To a mixture of sodium hydride (0.08 g) in 5 ml of tetrahydrofuran (THF) and 2 ml of hexamethylphosphoramide (HMPA), cooled in an ice bath, is added, dropwise, 2-methyl-2-[4-(1-methylpropoxy)phenoxy]ethanol (0.63 g). The mixture is stirred at RT for 2 hours, after which a solution of 2-chloropyridine (0.38 g) in 5 ml of THF is added and the mixture is stirred at 60° for 3 hours. The THF is then removed by rotoevaporation and the residue is purified by column chromatography on silica gel to give the product, 2-{2-methyl-2-[4-(1-methylpropoxy)phenoxy]ethoxy}pyridine, MS m/e 302 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389651 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-abefba7c21d548cf8df10c9700c80eab |
| Source note | uspto-grants-1995_02 |