HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Ethoxy-5-dimethylsilylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorodimethylsilane | HCID 66108 | — |
| Reactant | 5-Bromo-2-ethoxypyridine | HCID 817237 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Ethoxy-5-dimethylsilylpyridine | HCID 131715724 | 43% |
Reaction Steps
A mixture of 18.2 g (0.09 mol) of 2-ethoxy-5-bromopyridine (can be obtained from 2,5-dibromopyridine and sodium methanolate in DMSO), 11.4 g (0.12 mol) of chlorodimethylsilane and 50 ml of anhydrous tetrahydrofuran (THF) is added dropwise to 2.4 g (0.10 mol) of magnesium turnings in 10 ml of anhydrous THF, a strongly exothermic reaction occurring. The reaction is completed by refluxing for two hours. The mixture is then poured into water and extracted repeatedly with n-hexane, The extracts are washed with water and saturated sodium chloride solution, dried and evaporated, and the residue is distilled. 7 g (43%) of 2-ethoxy-5-dimethylsilylpyridine are obtained as a colorless oil of boiling point 7=140°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04775664 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-bb79b63bca1945fb99b09014ed8b4eab |
| Source note | uspto-grants-1988_10 |