HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyl phosphite → HCID 178460916, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyl phosphite | HCID 31215 | — |
| Reactant | HCID 123804129 | HCID 123804129 | — |
| Reactant | HCID 178505500 | HCID 178505500 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178460916 | HCID 178460916 | 36% |
Reaction Steps
A 25 ml THF solution of 1.0M 4-(4-(3,4-difluorophenyl)phenyl)cyclohexyl magnesium bromide (25 mmol) was dripped into a mixed solution of 5.36 g (20.0 mmol) of 4-iodo-1-n-propyl-1-silacyclohexane, 50 mg of copper (I) iodide, 100 mg of triethyl phosphite and 50 ml of THF. The silacyclohexane rings of the product thus obtained were a mixture of trans isomers and cis isomers. After a conventional after treatment, they were separated by means of chromatography to obtain 1.49 g (yield 36%) of the target product, i.e. the trans, trans isomers. The obtained target product exhibited the same physical properties as the product of Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05582764 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-c9b4909f2e1844fdabf2497940194c9b |
| Source note | uspto-grants-1996_12 |