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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449788Generated: October 25, 2026

Tetrahydrofuran → HCID 86682691, compound

https://huagongshe.com/reaction/449788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant4-CyclohexylresorcinolHCID 75055—
Reactant(Chloro(phenylmethoxy)phosphoryl)oxymethylbenzeneHCID 4641201—
SolventWaterHCID 962—
ProductHCID 86682691HCID 8668269164%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a tetrahydrofuran solution (10 ml) of 4-cyclohexylresorcinol (926 mg), sodium hydride (60% dispersion in liquid paraffin) (404 mg) was added and stirred at 0° C. for 30 minutes. Then, dibenzyl chlorophosphate (10 w/v % solution in benzene) (30 ml) was added dropwise. After stirring at room temperature for 3 hours, water (30 ml) was added to the reaction mixture, and the extraction was carried out with ethyl acetate (30 ml). Then, the extract was washed with saturated brine (20 ml), dried with anhydrous sodium sulfate and then concentrated. The residue (4.12 g) was subjected to silica gel chromatography (silica gel 90 g, chloroform to chloroform:methanol=100:1), to give 1,3-bis(dibenzylphosphonooxy)-4-cyclohexylbenzene (2.19 g, yield: 64%) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486919B2
Source datasetuspto-grants-2013_07
ORD IDord-e3fe8978e03448e5b19ee71f2e107697
Source noteuspto-grants-2013_07