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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964776Generated: October 26, 2026

Hydrochloric Acid → 2-Ethyl-4-phenyl-1-indanone

https://huagongshe.com/reaction/964776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantThionyl ChlorideHCID 24386—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3-(2-Biphenylyl)-2-ethylpropionic acidHCID 21571983—
Product2-Ethyl-4-phenyl-1-indanoneHCID 2217321885%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 236 g (0.93 mol) of 13 in 81 cm3 (1.2 mol) of thionyl chloride was stirred at room temperature for 18 hours. Excess thionyl chloride was removed at 10 mbar and the oily residue was freed from adhering residues of thionyl chloride by repeated dissolution in 200 cm3 of toluene in each case and stripping off in vacuo. The acid chloride was taken up in 400 cm3 of toluene and added dropwise at 10° C. to a suspension of 133 g (1.0 mol) of AlCl3 in 2000 cm3 of toluene. The reaction mixture was heated at 80° C. for 1 hour, poured into 2000 g of ice and acidified to pH 1 by means of concentrated aqueous HCl. The organic phase was separated off, and the aqueous phase was then extracted three times with 200 cm3 of Et2O in each case. The combined organic phases were washed with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution and subsequently dried (MgSO4), giving 187 g (85%) of 14, which was reacted further without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770753
Source datasetuspto-grants-1998_06
ORD IDord-cbfd08e87ed24727b7e94e64147d009a
Source noteuspto-grants-1998_06