Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2272520Generated: November 3, 2026

Sodium Thiosulfate → 5-Bromo-4-cyclopropyl-3-fluoro-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/2272520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantDibromoisocyanuric acidHCID 192912—
Reactant4-Cyclopropyl-3-fluoro-2-hydroxybenzaldehydeHCID 90423572—
SolventDimethylformamideHCID 6228—
Product5-Bromo-4-cyclopropyl-3-fluoro-2-hydroxybenzaldehydeHCID 90423491134%

Reaction Steps

Dibromoisocyanuric acid (1.43 g) was added at room temperature to a DMF (50 mL) solution of 4-cyclopropyl-3-fluoro-2-hydroxybenzaldehyde (1.50 g), and the mixture was stirred at the same temperature as above for 3 hours in a nitrogen atmosphere. A saturated aqueous solution of sodium thiosulfate was added to the reaction mixture at room temperature, followed by extraction with ethyl acetate. The obtained organic layer was washed with water and saturated saline in this order and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (1.73 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120777B2
Source datasetuspto-grants-2015_09
ORD IDord-0588c618ad6544ed9a671be368693346
Source noteuspto-grants-2015_09