HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Ethyl-4-p-tolyl-4-silacyclohexanone → 4-(4-(4-Fluorophenyl)phenyl)-1-ethyl-1-p-tolyl-1-silacyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Ethyl-4-p-tolyl-4-silacyclohexanone | HCID 19039156 | — |
| Reactant | HCID 178505512 | HCID 178505512 | — |
| Product | 4-(4-(4-Fluorophenyl)phenyl)-1-ethyl-1-p-tolyl-1-silacyclohexane | HCID 19039155 | — |
Reaction Steps
Using the same method as Example 14, 23.2 g of 4-ethyl-4-p-tolyl-4-silacyclohexanone was reacted with 4-(4-fluorophenyl)phenyl magnesium bromide; the alcohol generated was treated with a dehydration reaction followed by catalytic reduction to obtain 4-(4-(4-fluorophenyl)phenyl)-1-ethyl-1-p-tolyl-1-silacyclohexane; this was then reacted with iodine monochloride; and then the product was reduced using lithium aluminum hydride to obtain 2.12 g (yield 71%) of the target product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05641431 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-2d59a15dab2c46cb967a87f17e8a6ddc |
| Source note | uspto-grants-1997_06 |