HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 54462554, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium cyclohexylisopropylamide | HCID 10877271 | — |
| Reactant | HCID 14261111 | HCID 14261111 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54462554 | HCID 54462554 | — |
Reaction Steps
To a solution, prepared as described in (a), of 6 mmol of lithium cyclohexylisopropylamide in abs. THF there are added dropwise, at -78°, first 2.3 ml (18 mmol) of trimethylchlorosilane and then 1.2 g (5 mmol) of isovaleric acid 1-cyclohexyl-3-buten-2-yl ester. The solution is maintained at -78° for 1 hour, heated to room temperature over a period of 11/2 hours and stirred at that temperature for 1 hours. the reaction mixture is cooled to 0°, hydrolysed by adding 0.5 ml of methanol, diluted with ether, washed with 1N HCl and brine, dried over MgSO4 and concentrated by evaporation in a rotary evaporator. The residue is distilled as described in (a) and yields the same product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04898977 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-7529e245dc1e4601b83d66ba0732561a |
| Source note | uspto-grants-1990_02 |