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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877376Generated: October 31, 2026

2,5-Dichlorophenol → HCID 59294546, compound

https://huagongshe.com/reaction/1877376

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DichlorophenolHCID 66—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67366172HCID 67366172—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylacetamideHCID 31374—
ProductHCID 59294546HCID 5929454610%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of (3-bromo-pyridin-4-yl)-(3,4-dihydro-2H-quinolin-1-yl)-methanone (41.2 mg, 0.13 mmol, 1.0 equiv) and 2,5-dichloro-phenol (21.2 mg, 0.13 mmol, 1.0 equiv; [CAS RN 583-78-8]) in DMAc (1 mL) was added potassium carbonate (35.9 mg, 0.26 mmol, 2.0 equiv; [CAS RN 584-08-7]) and copper(I) iodide (5.0 mg, 0.026 mmol, 0.2 equiv; [CAS RN 7681-65-4]). The reaction mixture was heated by microwave irradiation to 180° C. for 8 h. Purification by preparative HPLC on reversed phase (Xterra® PrepMSC 18, 5 μm, 19×50 mm column equipped with a Gilson Liquid Handler 215 autosampler, two Rainin Dynamax® SD-300 pumps, a Sedex ELSD 75 lightscatter and a Dionex UVD 340S UV detector) eluting with a gradient of acetonitrile/water provided 5 mg (10%) of the title compound. MS (ISP): 399.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309734B2
Source datasetuspto-grants-2012_11
ORD IDord-c2fd8318dc7c4473a7bc8abdcac4bc15
Source noteuspto-grants-2012_11