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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097404Generated: October 29, 2026

Benzene → HCID 86657328, compound

https://huagongshe.com/reaction/1097404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantAcetyl diethyl phosphateHCID 18353—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzosuberoneHCID 70003—
ProductHCID 86657328HCID 86657328—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of sodium hydride (60%, 2.25 g) in anhydrous benzene (100 ml) was slowly added with a solution of diethyl phosphonoacetate (14.0 g) in anhydrous benzene (20 ml) at 0° C., and the mixture was stirred at 0° C. for 15 minutes. The mixture was added with a solution of 1-benzosuberone (5.00 g) in anhydrous benzene (30 ml), and the mixture was stirred at 0° C. for 15 minutes, and then refluxed overnight by heating. The reaction mixture was left to cool and then added with saturated aqueous ammonium chloride, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:200) to quantitatively obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143260B2
Source datasetuspto-grants-2012_03
ORD IDord-3b6dd7425ca34369a979590f0d38d2b6
Source noteuspto-grants-2012_03