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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417365Generated: November 1, 2026

Tetrahydrofuran → HCID 4115493, compound

https://huagongshe.com/reaction/2417365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCyclohexyl phenyl ketoneHCID 12837—
ReactantIodide IonHCID 30165—
ProductHCID 4115493HCID 4115493—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of methylbiphenylphosphonium iodide in dry THF cooled at 0° C. was added NaNH2. After stirring for 15 h at ambient temperature, cyclohexylphenyl ketone Was added. The reaction mixture was stirred for 8 h at ambient temperature and then quenched with aqueous ammonium chloride and extracted with ethyl acetate. The combined organic phases were washed (brine), dried (Na2SO4) and concentrated. Silica gel column chromatography of the crude product using petroleum ether:EtOAc (49:1) as eluent gave α-cyclohexylstyrene as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825378B2
Source datasetuspto-grants-2004_11
ORD IDord-25c94e98ef1d4caf83732f10246ce253
Source noteuspto-grants-2004_11