HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542633Generated: October 30, 2026
Chlorotrimethylsilane → [(Cyclooct-1-en-1-yl)oxy](trimethyl)silane
https://huagongshe.com/reaction/542633
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclooctanone | HCID 10403 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [(Cyclooct-1-en-1-yl)oxy](trimethyl)silane | HCID 54080585 | 80% |
Reaction Steps
To a solution of 42 g (0.38 mol) of chlorotrimethylsilane and 78 g of triethylamine in 100 ml of dimethylformamide, a solution of 32 g (0.254 mol) of cyclooctanone in 40 ml of dimethylformamide was added. The resultant mixture was stirred at 100° to 115° C. for 48 hours. At the end of the reaction, the reaction mixture was combined with 240 ml of n-hexane and washed twice with 300 ml of a saturated aqueous sodium bicarbonate solution. The mixture was washed under cooling with 180 ml of 1.5N hydrochloric acid, then washed sequentially with an aqueous sodium bicarbonate solution, water, and saline and then dried with magnesium sulfate. The mixture was concentrated and distilled under a vacuum, to afford 40 g (80% in yield) of 1-cyclooctenyloxytrimethylsilane having a boiling point of 82° to 84° C./5 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04658055 |
|---|
| Source dataset | uspto-grants-1987_04 |
|---|
| ORD ID | ord-097d42ba0f35440086fea782c76a27ad |
|---|
| Source note | uspto-grants-1987_04 |
|---|