HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Silane, (6-bromo-1-hexynyl)trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | HCID 10877568 | HCID 10877568 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Silane, (6-bromo-1-hexynyl)trimethyl- | HCID 11053532 | 125.8% |
Reaction Steps
To a mixture of 1-trimethylsilyl(hex-1-yn-6-ol) (32.6 g, 190 mmol) and pyridine (0.38 mL) dissolved in diethyl ether (100 mL) was added slowly phosphorus tribromide (7.1 mL, 75 mmol) in diethyl ether (20 mL). Upon addition a precipitate formed and the heterogeneous solution was stirred at room temperature overnight. The mixture was then heated at reflux for 2.5 hours and, upon cooling, was poured onto ice, washed with water, sodium bicarbonate solution, brine and dried (MgSO4). Evaporation of solvent under reduced pressure gave a residue which was distilled (b.p. 80° C., 3.5 mm Hg) to give 22 g (50%) of product. 1H NMR (CDCl3) δ: 0.14 (s, 9H), 1.64-1.72 (quintet, 2H), 1.91-2.02 (quintet, 2H), 2.27 (t, 2H), 3.44 (t, 2H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04877779 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-acd477e4cfe2484cbaa27803dce1b600 |
| Source note | uspto-grants-1989_10 |