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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817669Generated: October 25, 2026

Hydrochloric Acid → 1-(4'-Fluoro(1,1'-biphenyl)-4-yl)ethanone

https://huagongshe.com/reaction/1817669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantNitrobenzeneHCID 7416—
Reactant4-FluorobiphenylHCID 9461—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product1-(4'-Fluoro(1,1'-biphenyl)-4-yl)ethanoneHCID 608114—

Reaction Steps

4′-Fluoro-biphenyl (0.03 mol) was added to 1 M AlCl3 in nitrobenzene (40 mL, 0.04 mol) with chilling in an ice bath. Acetyl chloride (0.06 mol) was added dropwise and the mixture stirred overnight at room temperature. The dark solution was poured into a mixture of crushed ice (150 mL), water (25 mL) and HCl (50 mL). The aqueous phase was separated and the nitrobenzene removed by steam distillation to give a dark low melting solid. The solid was recrystallised from aqueous methanol to give the title compound. δC (CDCl3, 62.9 MHz): 26.7, 115.9 (d, J 21.5), 127.1, 129.0 (d, J=7.8), 135.8, 136.0 (d, J 2.9), 144.7, 163.0 (d, J 248.0) and 197.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598289B2
Source datasetuspto-grants-2009_10
ORD IDord-cfb0ceb716d94b1f9d53368872319c4d
Source noteuspto-grants-2009_10