HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377410Generated: October 31, 2026
Triethyl Phosphate → HCID 131720184, compound
https://huagongshe.com/reaction/1377410
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl Phosphate | HCID 6535 | — |
| Reactant | HCID 178455405 | HCID 178455405 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131720184 | HCID 131720184 | 37% |
Reaction Steps
33.5 g (0.1 mol) of 4-(4-bromocyclohexyl)-1-(1,2,2-trifluorovinyloxy)benzene was dropped in a mixture of 2.5 g (0.11 mols) of magnesium and 300 ml of THF to obtain a Grignard reagent. The resultant solution was then dropped in a solution, in 500 ml of THF, of 0.5 g of triethyl phosphate, 0.1 g of copper (I) iodide and 29.1 g (0.1 mol) of trans-4-(4-bromobutyl)-1-n-butyl-1-silacyclohexane. The resultant product consisted of a mixture of tram and cis isomers with respect to the cyclohexane ring. The product was subjected to ordinary aftertreatments to obtain trans-4-(4-(trans-4-(1,2,2-trifluorovinyloxy)phenyl)cyclohexyl)butyl)-1-n-butyl-1-silacyclohexane, followed by isolation through chromatography to obtain 17.1 g (yield: 37%) of the intended trans isomer product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665271 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-c6c3cd18dbee4b3ba103e141452faad9 |
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| Source note | uspto-grants-1997_09 |
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