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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707908Generated: October 25, 2026

Diethyl Ether → HCID 178418606, compound

https://huagongshe.com/reaction/1707908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 178418638HCID 178418638—
ReactantHCID 178418655HCID 178418655—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178418606HCID 178418606—

Reaction Steps

A solution of nonylmagnesium bromide (8.3 mmol) in 30 ml of diethyl ether was treated at 0° C. with a solution of 1.5 g of trans-4-(4'-cyano-4-biphenylyl)cyclohexyl tetrahydropyranyl ether in 15 ml of tetrahydrofuran. The reaction mixture was heated at slight reflux overnight and then treated with dilute sodium carbonate solution. The organic phase was separated and the aqueous phase was back-extracted three times with 50 ml of diethyl ether each time. The combined organic phases were washed once with dilute sodium carbonate solution and twice with water and then dried over magnesium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel with toluene/ethyl acetate (vol. 9;1). The trans-4-(4-decanoyl-4-biphenylyl)cyclohexyl tetrahydropyranyl ether (1.8 g) obtained was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356563
Source datasetuspto-grants-1994_10
ORD IDord-f1d4c58ea2694a9789de0df7ec4a8405
Source noteuspto-grants-1994_10