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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454224Generated: November 1, 2026

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

https://huagongshe.com/reaction/1454224

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 solids were 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 numberUS07479493B2
Source datasetuspto-grants-2009_01
ORD IDord-c2123d84604242fc8d6495a7e20bed67
Source noteuspto-grants-2009_01