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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333837Generated: October 30, 2026

Water → [1-(4-Chloro-phenyl)-cyclopropyl]-quinolin-3-yl-methanone

https://huagongshe.com/reaction/333837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-BromoquinolineHCID 21413—
Reactant1-(p-Chlorophenyl)cyclopropanecarbonitrileHCID 98666—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product[1-(4-Chloro-phenyl)-cyclopropyl]-quinolin-3-yl-methanoneHCID 66813279—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of n-butyl lithium (1.6 M in hexanes, 1.5 ml) was added to 3-bromoquinoline (CAS Reg. No. 5332-24-1) (500 mg) in diethyl ether (16 ml) at −78° C. The mixture was stirred at −78° C. for 1 h. A solution of 1-(4-chlorophenyl)-1-cyclopropanecarbonitrile (CAS Reg. No. 64399-27-5) (427 mg) in 3 ml diethyl ether was added at −78° C. to the red mixture and then stirred for 15 min at −78° C. The mixture was allowed to warm to room temperature, then poured into water (40 ml) and extracted with diethyl ether. The combined organic layers were dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, ethyl acetate/heptane 0:100-20:80, then ethyl acetate/DCM 0:100-10:90) to give the title compound as a light yellow oil (100 mg). MS (m/e)=308.3 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883786B2
Source datasetuspto-grants-2014_11
ORD IDord-a9765258f8bf4b2caa4f0bae9ec8e73d
Source noteuspto-grants-2014_11