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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588879Generated: November 4, 2026

Magnesium → 1-Cyclopropyl-1-(4-chlorophenyl)-4-cyano-4-(3-phenoxyphenyl)butane

https://huagongshe.com/reaction/1588879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMagnesiumHCID 5462224—
Reactant1-Cyclopropyl-1-(4-chlorophenyl)-4-cyano-4-(3-phenoxyphenyl)-3-buteneHCID 54410720—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product1-Cyclopropyl-1-(4-chlorophenyl)-4-cyano-4-(3-phenoxyphenyl)butaneHCID 1975485987.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.9 gram (0.002 mole) of 1-cyclopropyl-1-(4-chlorophenyl) -4-cyano-4-(3-phenoxyphenyl)-3-butene in 15 ml of methanol was stirred, and 0.5 gram (0.002 mole) of magnesium was added. The reaction mixture was stirred for about one hour at which time an exothermic reaction occurred. The reaction mixture was cooled to 0° C. where it was stirred for one hour, and then it was allowed to warm to ambient temperature where it stirred for two hours. After this time the reaction mixture was diluted with 20 ml of aqueous 10% hydrochloric acid, and the mixture was extracted with diethyl ether. The combined extracts were dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 0.7 gram of 1-cyclopropyl-1-(4-chlorophenyl)-4-cyano-4-(3-phenoxyphenyl)butane. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05223536
Source datasetuspto-grants-1993_06
ORD IDord-e8ef1404c248414b9abcee41d4f2b800
Source noteuspto-grants-1993_06