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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248145Generated: October 27, 2026

1-Bromopropane → 1-[1-(3-Chloro-5-methylphenyl)cyclobutyl]butylamine hydrochloride

https://huagongshe.com/reaction/1248145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopropaneHCID 7840—
ReactantMagnesiumHCID 5462224—
Reactant1-(3-Chloro-5-methylphenyl)-1-cyclobutanecarbonitrileHCID 21294830—
ReactantHCID 178455851HCID 178455851—
SolventDiethyl EtherHCID 3283—
Product1-[1-(3-Chloro-5-methylphenyl)cyclobutyl]butylamine hydrochlorideHCID 13083306—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 1-(3-chloro-5-methylphenyl)-1-cyclobutanecarbonitrile (8.0 g) in ether (40 ml) was added to a solution of propyl magnesium bromide [prepared by the reaction of 1-bromopropane (6.7 g) and magnesium (1.3 g)] in ether (80 ml) and the mixture heated under reflux for two and a half hours. Two thirds of the ether was evaporated off and then, after cooling, a solution of sodium borohydride (3.5 g) in ethanol (150 ml) added. The mixture was maintained at 50° C. for one hour and water (50 ml) and then 5N hydrochloric acid (50 ml) added. The ether layer was separated, dried and evaporated to yield a solid which was recrystallised from propan-2-ol to give 1-[1-(3-chloro-5-methylphenyl)cyclobutyl]butylamine hydrochloride (m.p. 145°-146° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522828
Source datasetuspto-grants-1985_06
ORD IDord-70c06149320242169d141ae7bf792bb2
Source noteuspto-grants-1985_06