HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → HCID 19801182, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | HCID 19801174 | HCID 19801174 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19801182 | HCID 19801182 | — |
Reaction Steps
1.24 ml of diisopropylamine and 6 ml of tetrahydrofuran are cooled to -40° C., then 4.7 ml of butyllithium is added drop by drop. The temperature is allowed to rise to -20° C., agitation is carried out for 1/4 hour, then 1 g of 4-(2-propenyl)-1-indanone in 10 ml of tetrahydrofuran is introduced at -70° C. After agitation for one hour at -60° C., 1.15 ml of trimethylsilyl chloride in 6 ml of tetrahydrofuran is added, with agitation for one hour at -60° C. The mixture is poured over 100 ml of water and ice and 100 ml of ether. After decanting, the aqueous phase is extracted with ether, the organic phases are reunited, dried and concentrated to dryness without heating, and 1.51 g of expected product is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05180741 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-f3bb77fb21a14bc19754733118689c8c |
| Source note | uspto-grants-1993_01 |