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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071969Generated: October 31, 2026

Ammonium Chloride → 2-(3,5-Dimethoxyphenyl)-5-(p-fluorophenyl)pentane

https://huagongshe.com/reaction/2071969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(3,5-Dimethoxyphenyl)ethan-1-oneHCID 95997—
ReactantMagnesiumHCID 5462224—
Reactant1-(3-Bromopropyl)-4-fluorobenzeneHCID 14737133—
CatalystPalladiumHCID 23938—
SolventDiethyl EtherHCID 3283—
SolventEthanol hydrochlorideHCID 21887872—
Product2-(3,5-Dimethoxyphenyl)-5-(p-fluorophenyl)pentaneHCID 20287872—

Reaction Steps

A solution of 77 g. of 3-(4-fluorophenyl)propylbromide in 300 ml. of ether was added dropwise over a two hour period to a refluxing solution of 10 g. of magnesium in 100 ml. of ether. The reaction mixture was refluxed for an additional 30 minutes after the addition was completed. A solution of 68 g. of 3,5-dimethoxyacetophenone in 100 ml. of ether was then added dropwise to the reaction and the reaction mixture was refluxed for 11/2 hours. To the reaction was added 300 ml. of a saturated ammonium chloride solution dropwise with stirring. The layers were separated and the aqueous layer extracted with ether. The ether extract was dried over magnesium sulfate and the ether removed in vacuo to give an oil. An additional 111.7 g. of 3(4-fluorophenyl) propylbromide was reacted with 3.5-dimethoxyacetophenone in the above manner. The products from both runs were hydrogenated in ethanol-HCl using palladium as the catalyst. The solvents and catalyst were removed and the crude material distilled to yield 169.0 g. of 2-(3,5-dimethoxyphenyl)-5-(4-p-fluorophenyl)pentane, b.p. 145 - 155/0.05 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049653
Source datasetuspto-grants-1977_09
ORD IDord-47d043b0498e4aec9373d2abe8520a89
Source noteuspto-grants-1977_09