HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylacetylene → BIS(PHENYLETHYNYL)DIMETHYLSILANE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Chlorodimethylsilane | HCID 66108 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | BIS(PHENYLETHYNYL)DIMETHYLSILANE | HCID 11010735 | — |
Reaction Steps
To 50 ml of tetrahydrofuran (THF) solution containing 6 ml of ethynylbenzene, 33 ml of 1.6N normal-butyl lithium was added dropwise under a nitrogen gas flow at 0° C. After stirring for 1 hour, 33.3 ml of THF solution containing 3 ml of dimethylsilyl chloride was added. After stirring at the room temperature for one night, the deposited solid was filtered and thereafter the obtained reaction solution was concentrated. Water was added to the solution, and then the solution was extracted with diethyl ether. Furthermore, the said diethyl ether layer was washed with water, thereafter dried with magnesium sulfate and concentrated. Then it was recrystallized from hexane, to obtain 5.02 g of bisphenylethynyldimethylsilane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06051319 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-34e7ae6c961b45c382b46bd3ef47f406 |
| Source note | uspto-grants-2000_04 |