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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197921Generated: October 30, 2026

3-Hydroxybenzaldehyde → 3-(4-Chloro-2-nitro-phenoxy)-benzaldehyde

https://huagongshe.com/reaction/2197921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-chloronitrobenzeneHCID 2794904—
SolventDimethylformamideHCID 6228—
Product3-(4-Chloro-2-nitro-phenoxy)-benzaldehydeHCID 928134141%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of DMF (50 mL) was added 1-bromo-2-nitro-4-chloro-benzene (10.0 g, 42.2 mmol), 3-hydroxybenzaldehyde (5.2 g, 42.2 mmol), and K2CO3 (11.5 g, 84.6 mmol). The solution was heated to 85° C. and stirred overnight. The reaction was poured into distill water and extracted with ethyl acetate. The combined organic layers were washed with distilled water, brine, and dried over Na2SO4, filtered and concentrated under vacuum giving the crude title compound. This solid was purified by silica gel column chromatography eluting with hexanes/ethyl acetate (4:1) to give the title compound (4.4 gm, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338605B2
Source datasetuspto-grants-2012_12
ORD IDord-ac4c381a28564f6c81080513ace2b1f2
Source noteuspto-grants-2012_12