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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080587Generated: November 1, 2026

Triethyl Phosphate → HCID 178455407, compound

https://huagongshe.com/reaction/1080587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl PhosphateHCID 6535—
ReactantMagnesiumHCID 5462224—
ReactantHCID 23364723HCID 23364723—
ReactantHCID 178455404HCID 178455404—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178455407HCID 17845540772.6%

Reaction Steps

36.9 g (0.1 mol) of 4-(4-bromocyclohexyl)-2,3',4'-trifluorobiphenyl 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 26.3 g (0.1 mol) of trans-1-(2-bromoethyl)-4-n-butyl-4-silacyclohexane. After a conventional after treatment, 4-(trans-4-(2-(trans-4-n-butyl-4-silacyclohexyl)ethyl)cyclohexyl)-2,3',4'-trifluorobiphenyl 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 34.3 g (yield 72.6%) of the trans isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05582764
Source datasetuspto-grants-1996_12
ORD IDord-99ab53a6d73640a9b8d719c06ec392b4
Source noteuspto-grants-1996_12