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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36824Generated: October 25, 2026

Acetyl chloride → 1-Acetyl-4-(4-phenylphenyl)benzene

https://huagongshe.com/reaction/36824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantO-TerphenylHCID 6766—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
Product1-Acetyl-4-(4-phenylphenyl)benzeneHCID 3744472119%

Reaction Conditions

Temperature-5 °C

Reaction Steps

After a mixture of 172 g of terphenyl, 860 ml of benzene, and 353 g of acetyl chloride was cooled to -5° C., it was added with a total of 200 g of anhydrous aluminium chloride in few instalments, and subjected to reaction at -5° C. for 1 hour and further at 10° C. for 1 hour. The solid materials thus formed were separated by filtration, washed with a total of 4 liter of methanol in few instalments, and then recrystallized from chloroform to obtain 121 g of 4-acetyl-p-terphenyl, 2. The yield was 59%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05417885
Source datasetuspto-grants-1995_05
ORD IDord-fcf69c324b7543df958050b25c92f785
Source noteuspto-grants-1995_05