HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 6-Methoxythieno[3,2-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Thieno[3,2-b]pyridin-6-ol | HCID 20148567 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 6-Methoxythieno[3,2-b]pyridine | HCID 20148582 | 78.5% |
Reaction Steps
To a solution of 6-hydroxythieno[3,2-b]pyridine (2.45 g, 16.2 mmol) in dry dimethylsulfoxide (15 ml), under a nitrogen atmosphere, was added 60% sodium hydride in mineral oil (0.75 g, 19 mmol) and let stir at room temperature for 1 hour. Methyl iodide (1.25 ml, 21 mmol) was added to this solution and it was stirred for an additional two hours. The solution was poured into ice/water and extracted with diethyl ether, washed with water, dried over anhydrous sodium sulfate, filtered and carefully evaporated to give an oily product (2.1 g, 78% yield) which was used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731368 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-5e4ad5e54b854f339997a2ef5d46f549 |
| Source note | uspto-grants-1988_03 |