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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444358Generated: October 30, 2026

Hydrochloric Acid → 2-(3-Methoxyphenyl)-5-phenylpentane

https://huagongshe.com/reaction/444358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantDiethyl EtherHCID 3283—
Reactant(1-Bromopropyl)benzeneHCID 562384—
ReactantMagnesiumHCID 5462224—
CatalystPalladiumHCID 23938—
Product2-(3-Methoxyphenyl)-5-phenylpentaneHCID 20496826—

Reaction Steps

A solution of 1-bromopropylbenzene (51.7 g.) in ether (234 ml.) is added dropwise over a 2-hour period to a refluxing mixture of magnesium (7.32 g.) in ether (78 ml.). The reaction mixture is refluxed for 30 minutes longer and then a solution of 3-methoxy-acetophenone (41.6 g.) in ether (78 ml.) is added dropwise and the mixture heated to reflux for 1.5 hours. The reaction is quenched by addition of saturated ammonium chloride (234 ml.), the ether layer is separated and the aqueous phase extracted with ether (3×200 ml.). The combined ether extracts are dried over magnesium sulfate and concentrated under vacuum to yield an oil. The oil is hydrogenated in a mixture containing ethanol (300 ml.) , concentrated hydrochloric acid (2 ml.) and 5% palladium-on-carbon (5 g.). The catalyst is filtered off and the ethanol removed under vacuum. The residue is distilled under vacuum to give the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04263438
Source datasetuspto-grants-1981_04
ORD IDord-fbaa76584e2644f894c38b2d046c8e94
Source noteuspto-grants-1981_04