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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232424Generated: November 1, 2026

Benzonitrile, 3-(bromomethyl)- → 3-(2-(7-Chloroquinolin-2-yl)ethyl)benzonitrile

https://huagongshe.com/reaction/232424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzonitrile, 3-(bromomethyl)-HCID 97249—
Reactant7-Chloro-2-methylquinolineHCID 138395—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product3-(2-(7-Chloroquinolin-2-yl)ethyl)benzonitrileHCID 9994506—

Reaction Steps

To a solution of 7-chloroquinaldine (17.7 g) in THF (80 mL) at -78° was added a solution of 100 mL lithium diisopropyl amide (LDA) (1M) dropwise. After addition the solution was warmed to -20° and added dropwise to 3-cyanobenzyl bromide (20 g) in THF (80 mL) at 0°. The reaction mixture was stirred 1 hr at 0° and warmed to room temperature (30 min). The mixture was partitioned between pH 7 buffer (25% NH4OAc) and ethyl acetate. The organic layer was dried and evaporated. Flash chromatography of the residue using 30% ether in hexane afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851409
Source datasetuspto-grants-1989_07
ORD IDord-b1335a9bf3674e7ea6bec533d92e00e8
Source noteuspto-grants-1989_07