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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877377Generated: November 1, 2026

2,5-Dichlorophenol → HCID 29042269, compound

https://huagongshe.com/reaction/1877377

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DichlorophenolHCID 66—
ReactantHydrochloric AcidHCID 313—
Reactant2-Iodobenzoic acidHCID 6941—
ReactantCesium carbonateHCID 10796—
Catalysttetrakis(acetonitrile)copper(I) hexafluorophosphateHCID 11068737—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 29042269HCID 29042269—

Reaction Steps

To a solution of 2-iodo-benzoic acid (3.0 g, 12.10 mmol, 1.0 equiv; [CAS RN 88-67-5]) and 2,5-dichloro-phenol (1.97 g, 12.10 mmol, 1.0 equiv; [CAS RN 583-78-8]) in toluene (50 mL) was added caesium carbonate (7.88 g, 24.20 mmol, 2.0 equiv; [CAS RN 534-17-8]) and tetrakis(acetonitrile)copper(I) hexafluorophosphate (1.13 g, 3.02 mmol, 0.25 equiv; [CAS RN 64443-05-6]). The reaction mixture was heated to reflux over night. The solvent was evaporated under reduced pressure and the crude reaction product taken up in water (100 mL), acidified to pH 1 by addition of a solution of 1 M HCl and extracted with ethyl acetate (3×100 mL). The combined organic phases were dried over MgSO4 and the product purified by silica column chromatography using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of heptane (+1% acetic acid)/ethyl acetate affording 2.78 g (81%) of the title compound as a white solid. MS (ISN): 281.1 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309734B2
Source datasetuspto-grants-2012_11
ORD IDord-3e595f77645b4d299a4bcbd25d1d7ba2
Source noteuspto-grants-2012_11