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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283631Generated: October 31, 2026

4-Acetyl-4'-chlorobiphenyl → 4-Chloro-4'-ethyl-1,1'-biphenyl

https://huagongshe.com/reaction/1283631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Acetyl-4'-chlorobiphenylHCID 592569—
Reactant1-(2′-Chloro[1,1′-biphenyl]-4-yl)ethanoneHCID 612000—
ReactantHCID 178418361HCID 178418361—
SolventBenzeneHCID 241—
Product4-Chloro-4'-ethyl-1,1'-biphenylHCID 13270640—

Reaction Steps

The procedure of Example 3 was repeated, except that the 4'-(2-chlorophenyl)acetophenone was replaced with an equal amount of 4'-(4-chlorophenyl)acetophenone, the amount of benzene employed was increased to 200 ml, and the amount of sulfuric was reduced to 5 drops. After seven hours, hydrogen pressure had dropped to 35.5 psig. Evaporation of the benzene left a solid which, according to nuclear magnetic resonance analysis, contained only about 67 percent of the desired ethylbenzene. Consequently, the solid was subjected to the hydrogenation procedure again, using 200 ml of benzene, 2 g of catalyst, and 1 ml of concentrated sulfuric acid. The solid obtained upon evaporation of the benzene was recrystallized from hexane, giving 1-ethyl-4-(4-chlorophenyl)benzene, mp 103°-127 104°. The following elemental analysis was obtained:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975542
Source datasetuspto-grants-1976_08
ORD IDord-d84cbbcf2e2c418f83465ca03108086d
Source noteuspto-grants-1976_08