HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Silane, (6-iodo-1-hexynyl)trimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | (6-Chlorohex-1-yn-1-yl)trimethylsilane | HCID 13839479 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Silane, (6-iodo-1-hexynyl)trimethyl- | HCID 10401411 | 96.2% |
Reaction Steps
A mixture of 6-chloro-1-trimethylsilylhex-1-yne (14.0 g.) and sodium iodide (30 g) in butanone (100 ml) was heated at reflux, with stirring, for 10 hours. After this time the solvent was removed in vacuo and the residue partitioned between diethyl ether and water. The organic phase was separated, washed with water and brine before drying over anhydrous magnesium sulphate. The solvent was removed under reduced pressure to leave 6-iodo-1-trimethylsilylhex-1-yne as a yellow oil (20.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026874 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-a022c1d44b674bacaf3d6ab58209792b |
| Source note | uspto-grants-1991_06 |