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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728053Generated: October 26, 2026

Hydrochloric Acid → 1-(4-Methoxyphenyl)-2-phenylethan-1-one

https://huagongshe.com/reaction/728053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnisoleHCID 7519—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
SolventChloroform methanolHCID 21584188—
Product1-(4-Methoxyphenyl)-2-phenylethan-1-oneHCID 231093—

Reaction Steps

To 10.8 g (0.10 mole) methoxybenzene and 13.9 g. (0.09 mole) phenylacetyl chloride in 1.0 1. methylene chloride there are added, by small amounts, 13.3 g. (0.10 mole) aluminium chloride at room temperature and with strong agitation. The reaction mixture is agitated for a further 2 hours and then is poured onto ice and 50 ml. hydrochloric acid are added. After separation of the organic phase, the aqueous solution is shaken out twice with 500 ml. methylene chloride each time, the combined organic phases are washed with water and the solvent is removed in vacuo. The smeary residue is freed of the volatile components by steam distillation and the remaining solid is crystallized from ethanol after filtration and washing with water. Obtained are colorless crystals having a melting point of 75° C.; Rf 0.7 [CHCl3 /CH3OH (9/1)]; yield: 18.3 g. (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05047431
Source datasetuspto-grants-1991_09
ORD IDord-34a3d8d523ea4bd2a7229b76f02fe631
Source noteuspto-grants-1991_09