HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → (R)-tert-butyldimethyl(1-methylcyclohex-2-enyloxy)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (R)-1-methylcyclohex-2-enol | HCID 11094567 | — |
| Reactant | 4H-Imidazole | HCID 12744656 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (R)-tert-butyldimethyl(1-methylcyclohex-2-enyloxy)silane | HCID 68008146 | — |
Reaction Steps
To a solution of (R)-1-methylcyclohex-2-enol, 50a, (1.00 g, 8.91 mmol) in 20 dry DMF at room temperature was added 4H-imidazole (1.82 g, 26.74 mmol), tert-butyldimethylchlorosilane (2.02 g, 13.33 mmol) and a catalytic amount of 4-dimethylaminopyridine (0.11 g, 0.89 mmol). The resulting mixture was stirred at room temperature overnight. It was then diluted with ether, washed consecutively with water, citric acid and water. The organic phase was dried with MgSO4, filtered and concentrated in vacuo. The colorless crude oil 1.98 g was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829007B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-d8e9a94d9dc5491ba892b5f4ccd25b07 |
| Source note | uspto-grants-2014_09 |