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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361467Generated: October 30, 2026

1,2-Dichloro-4-nitrobenzene → 2-Chloro-1-(4-chlorobenzyloxy)-4-nitrobenzene

https://huagongshe.com/reaction/1361467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dichloro-4-nitrobenzeneHCID 7443—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorobenzyl alcoholHCID 13397—
SolventDimethylacetamideHCID 31374—
Product2-Chloro-1-(4-chlorobenzyloxy)-4-nitrobenzeneHCID 6692192246.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

N,N-Dimethylacetamide (42 mL), 16.2 g of 1,2-dichloro-4-nitrobenzene, 12 g of 4-chlorobenzyl alcohol, and 8.7 g of potassium carbonate were mixed together, and the mixture was stirred with heating at 100 to 140° C. for 30 hr. This reaction solution was concentrated under the reduced pressure. The residue was dissolved in 100 mL of ethyl acetate and 100 mL of toluene, and the solution was washed with water and brine. The organic layer was concentrated under the reduced pressure, and the residue was recrystallized from ethanol to give 11.77 g of 2-chloro-1-(4-chlorobenzyloxy)-4-nitrobenzene (yield 46.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880006B2
Source datasetuspto-grants-2011_02
ORD IDord-8f3e5a6aa3a64f26a10b7bddc406421d
Source noteuspto-grants-2011_02