HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 6-Methyl-2,3-dihydro-[1,4]dioxino[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(2-Iodo-6-methylpyridin-3-yloxy)ethanol | HCID 21873798 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Methyl-2,3-dihydro-[1,4]dioxino[2,3-b]pyridine | HCID 15633299 | 16% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a stirred solution of 2-(2-iodo-6-methylpyridin-3-yloxy)ethanol (350 g, 1.25 mol) in anhydrous DMF (3.5 L) was added NaH (60 g, 1.5 mol), Cu (33.7 g, 0.53 mol) and CuSO4 (100 g, 0.63 mol) at 0° C. After the addition, the mixture was stirred at 100° C. overnight. After cooling, the solvent was removed in vacuo and the residue was diluted with water (1.5 L). The aqueous solution was extracted with CH2Cl2 (3×350 mL). The combined organic layers were washed with brine (2×100 mL), dried over anhydrous Na2SO4 and concentrated. The residue was purified via column chromatography (silica gel, EtOAc/petroleum ether 1:20) to yield 6-methyl-2,3-dihydro-[1,4]dioxino[2,3-b]pyridine (30.0 g, 16%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609680B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-0bcda9c1a9c4405ba511c9d962c19165 |
| Source note | uspto-grants-2013_12 |