Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38241Generated: October 25, 2026

3-Chlorophenol → 2-Chloro-1-(3-chlorophenoxy)-4-nitrobenzene

https://huagongshe.com/reaction/38241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorophenolHCID 7933—
ReactantCesium carbonateHCID 10796—
Reactant2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
Solventacetonitrile N,N-dimethylformamideHCID 21891449—
Product2-Chloro-1-(3-chlorophenoxy)-4-nitrobenzeneHCID 275207100%

Reaction Steps

According to Scheme 3 Step 1, Method A: 2-Chloro-1-fluoro-4-nitrobenzene (1.12 mmol, 0.20 g) was added to a suspension of 3-chlorophenol (1.02 mmol, 0.10 mL), Cs2CO3 (1.25 mmol, 407 mg) in DMF/ACN (40:60, 3.6 mL). The reaction mixture was stirred at room temperature overnight. The reaction mixture was quenched with water. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over MgSO4, was filtered and was concentrated under reduced pressure. The crude product was used without further purification to obtain 2-chloro-1-(3-chlorophenoxy)-4-nitrobenzene (1.02 mmol, 288 mg, 100%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524726B2
Source datasetuspto-grants-2013_09
ORD IDord-b52fe3e2f3204a35b4cfbbf66d690716
Source noteuspto-grants-2013_09