Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019793Generated: November 1, 2026

2-Chloro-7-fluoroquinoline-3-carbaldehyde → 1-(2-Chloro-7-fluoroquinolin-3-yl)ethanol

https://huagongshe.com/reaction/1019793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-7-fluoroquinoline-3-carbaldehydeHCID 12099179—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Chloro-7-fluoroquinolin-3-yl)ethanolHCID 24276077—

Reaction Steps

A suspension of 2-chloro-7-fluoroquinoline-3-carbaldehyde (44.7 g, 213 mmol) in THF (600 mL) was treated with MeMgBr (78.0 mL, 234 mmol 1.1 eq) at −20° C. After stirring overnight, the reaction was quenched with NH4Cl solution and extracted with Et2O (300 mL and 100 mL). The organic layers were washed with water, brine, dried over Na2SO4, concentrated and recrystallized from EtOAc (100 mL) and hexane (1 L). A pale yellow solid of 1-(2-chloro-7-fluoroquinolin-3-yl)-ethanol was obtained (41 g, 85%). Mass Spectrum (ESI) m/e=226 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716290B2
Source datasetuspto-grants-2014_05
ORD IDord-da16a28943044505b76803b6d18524d3
Source noteuspto-grants-2014_05