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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097407Generated: October 31, 2026

Benzene → HCID 66811298, compound

https://huagongshe.com/reaction/1097407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantAcetic acid, anhydride with diethyl hydrogen phosphateHCID 18353—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86657329HCID 86657329—
ProductHCID 66811298HCID 6681129894%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of sodium hydride (60%, 0.130 g) in anhydrous benzene (5 ml) was slowly added with diethyl phosphonoacetate (0.750 g) at 0° C., and the mixture was stirred at 0° C. for 10 minutes. The mixture was added with a solution of (6,7,8,9-tetrahydro-5H-5-benzocycloheptenyl)acetaldehyde (0.419 g) in anhydrous benzene (5 ml), and the mixture was stirred at 0° C. for 5 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=1:300) to obtain the title compound (0.544 g, yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143260B2
Source datasetuspto-grants-2012_03
ORD IDord-f0d2cc75700d4154a13c47813711669d
Source noteuspto-grants-2012_03