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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080586Generated: November 2, 2026

Triethyl Phosphate → HCID 19602027, compound

https://huagongshe.com/reaction/1080586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl PhosphateHCID 6535—
ReactantMagnesiumHCID 5462224—
ReactantHCID 123407593HCID 123407593—
ReactantHCID 178444391HCID 178444391—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19602027HCID 1960202790.1%

Reaction Steps

26.1 g (0.1 mol) of trans-1-(2-bromoethyl)-4-n-pentylcyclohexane 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 40.7 g (0.1 mol) of 4-(4-chloro-4-silacyclohexyl)3',5'-difluoro-4'-trifluoromethoxybiphenyl. After a conventional after treatment, 4-(2-(trans-4-n-pentylcyclohexyl)ethyl)-4-silacyclohexyl)-3',5'-difluoro-4'-trifluoromethoxybiphenyl 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 44.3 g (yield 90.1%) of the trans isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05582764
Source datasetuspto-grants-1996_12
ORD IDord-dbcfa363f8db4edc9ff73b6ccce0c2d3
Source noteuspto-grants-1996_12