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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232866Generated: October 25, 2026

7-Chloro-6-fluoro-2-formylquinoline → (7-Chloro-6-fluoroquinolin-2-yl)methanol

https://huagongshe.com/reaction/232866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-6-fluoro-2-formylquinolineHCID 23359173—
ReactantHCID 178418435HCID 178418435—
SolventMethanolHCID 887—
Product(7-Chloro-6-fluoroquinolin-2-yl)methanolHCID 2335911169.4%

Reaction Steps

3 g of sodium boron hydride was added to 11.19 g of 7-chloro-6-fluoro-2-formylquinoline obtained in Reference example 2 suspended in 250 ml of methanol and the mixture was stirred at room temperature for 1 hour. After the solvent was removed, the residue was extracted with ice water-methylene chloride and the organic layer was washed with water and dried over anhydrous sodium sulfate. After the solvent was removed, the residue was applied to silica gel column chromatography to obtain 7.84 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591752
Source datasetuspto-grants-1997_01
ORD IDord-20468624d1b34544a12da48e15e04df3
Source noteuspto-grants-1997_01