Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499001Generated: October 26, 2026

Water → 5-Bromo-2-(3,4-dichlorophenoxy)benzaldehyde

https://huagongshe.com/reaction/499001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4-DichlorophenolHCID 7258—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-fluorobenzaldehydeHCID 736327—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-(3,4-dichlorophenoxy)benzaldehydeHCID 1201703054%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 5-bromo-2-fluoro-benzaldehyde (5.13 g, 25.4 mmol) in DMF (25 mL) were added K2CO3 (7.15 g, 51.8 mmol) and 3,4-dichloro-phenol (4.67 g, 28.8 mmol). The mixture was heated at 90° C. for 24 h and then was allowed to cool to room temperature (rt). Water was added and the mixture was extracted with Et2O. The combined organic layers were dried (MgSO4) and concentrated. The residue was diluted with DCM and hexanes and the resulting solid was collected by vacuum filtration to provide the desired product (4.74 g, 54%). 1H NMR (CDCl3): 10.36 (s, 1H), 8.06 (d, J=2.5, 1H), 7.67 (dd, J=8.8, 2.6, 1H), 7.46 (d, J=8.8, 1H), 7.17 (d, J=2.8, 1H), 6.92 (dd, J=8.8, 2.8, 1H), 6.84 (d, J=8.8, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767666B2
Source datasetuspto-grants-2010_08
ORD IDord-be9a55e9995146bfb0ff4f06d5e42234
Source noteuspto-grants-2010_08