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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784445Generated: October 29, 2026

4-Chloro-3-methylphenol → HCID 86610739, compound

https://huagongshe.com/reaction/1784445

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-methylphenolHCID 1732—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86610737HCID 86610737—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86610739HCID 8661073984%

Reaction Steps

To a solution of potassium carbonate (115 mg, 0.83 mmol), potassium iodide (catalytic amount) and 4-chloro-m-cresol (65 mg, 0.46 mmol) in dimethylformamide (2 ml) was added a solution of 6-dimethylcarbamoyloxy-1-(R)-(2-bromoethyl)-3,4-dihydro-1H-isoquinoline-trifluoroacetamide (160 mg, 0.38 mmol) obtained in step (e) of Example 190 in dimethylformamide (2 ml) gradually with stirring under cooling in an ice bath. Subsequently, the resulting mixture was stirred at 100° C., and after confirming the disappearance of the starting material by thin layer chromatography, the reaction temperature was cooled to ambient temperature and water was added to the reaction mixture with stirring. The resulting mixture was extracted with ethyl acetate, and the extract was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (80:20) as the eluent to afford the title compound (154 mg, yield: 84%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504393B2
Source datasetuspto-grants-2009_03
ORD IDord-cf323f7afa53467cafe4b857cd8596b7
Source noteuspto-grants-2009_03