HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl Phosphate → HCID 178447755, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl Phosphate | HCID 6535 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 23364823 | HCID 23364823 | — |
| Reactant | HCID 178447742 | HCID 178447742 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178447755 | HCID 178447755 | 29.2% |
Reaction Steps
27.7 g (0.1 mol) of trans-1-(2-bromoethyl)-4-n-pentyl-4-silacyclohexane was dripped into a mixture of 2.5 g (0.11 mol) of magnesium and 300 ml of THF to obtain a Grignard's reagent. This solution was then dripped into a 500 ml THF solution of 0.5 g of triethyl phosphate, 0.1 g of copper (I) iodide and 35.1 g (0.1 mol) of 4-(4-bromocyclohexyl)-2,4'-difluorobiphenyl. After a conventional after treatment, 4-(trans-4-(2-(trans-4-n-pentyl-4-silacyclohexyl)ethyl)cyclohexyl)-2,4'-difluorobiphenyl was obtained. The silacyclohexane rings of the product were a mixture of trans isomers and cis isomers. They were separated by means of chromatography to obtain 13.1 g (yield 29.2%) of the trans isomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05582764 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-20d3af8928c54ff1b66d8c917d2a2a4a |
| Source note | uspto-grants-1996_12 |