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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975739Generated: October 29, 2026

Tetrahydrofuran → HCID 86748971, compound

https://huagongshe.com/reaction/975739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-(1,3-Dioxan-2-yl)ethyltriphenylphosphonium bromideHCID 2724168—
Reactant2-Methylpropan-2-olateHCID 4574913—
ReactantHCID 22915889HCID 22915889—
SolventDiethyl EtherHCID 3283—
ProductHCID 86748971HCID 86748971—

Reaction Steps

Into a three-necked flask equipped with a dropping funnel, a three-way cock and a thermometer was placed 2-(1,3-dioxan-2-yl)ethyltriphenylphosphonium bromide (22.9 g, 50 mmols), followed by adding tetrahydrofuran (100 ml), suspending, stirring the suspension under ice cooling till the liquid temperature reached 10° C. The resulting reaction mixture is added pottasium t-butoxide (5.6 g, 50 mmols), followed by elevating the temperature up to room temperature under ice cooling for one hour, stirring for one hour, dropwise adding a tetrahydrofuran (100 ml) solution of (4-(4-propylphenyl)phenyl)cyclohexanone (14.0 g, 48 mmols) over 30 minutes from the dropping funnel, further stirring the reaction liquid for 5 hours after completion of the dropwise addition, adding ether (200 ml), allowing to stand for one hour, filtering off deposited insoluble substance, concentrating the filtrate under reduced pressure and isolating and purifying the resulting pale brown oil by means of silica gel column chromatography, to obtain 1-(2-(1,3-dioxane-2-yl)ethylidene)-4-(4-(4-propylphenyl)-phenylcyclohexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05609791
Source datasetuspto-grants-1997_03
ORD IDord-ab879d2b16c4443389848964435964ee
Source noteuspto-grants-1997_03