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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100648Generated: November 1, 2026

Methyl iodide → HCID 57799915, compound

https://huagongshe.com/reaction/2100648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 57799945HCID 57799945—
SolventAcetonitrileHCID 6342—
ProductHCID 57799915HCID 5779991577.2%

Reaction Steps

To a stirred solution of crude 2-((dimethylamino)methyl)-3-(3-fluoro-2-methylphenyl)-1,5-bis(3-methoxyphenyl)-4-methylenepentane-1,5-dione (91 g, 186 mmol) in acetonitrile (769 mL) was added diisopropylethylamine (65 mL, 376 mmol) followed by iodomethane (140 mL, 2.24 mol). The mixture was stirred at room temperature for 16 h. To this mixture was added 2 M KOH (307 mL, 614 mmol), and the temperature was raised to 75° C. for 16 h. The mixture was partitioned between dichloromethane and water. The layers were separated and the aqueous phase extracted with 500 mL dichloromethane. The combined organic layers were dried over MgSO4, filtered, and evaporated to dryness. The residue was treated with 350 mL ether, isolated by filtration, and washed with 2×100 mL of ether. The ether layers were concentrated in vacuum to give 3-(3-fluoro-2-methylphenyl)-1,5-bis(3-methoxyphenyl)-2,4-dimethylenepentane-1,5-dione (63.8 g, 77% yield), (characterized by LCMS and 1H NMR). LRMS (M+H+) m/z=445.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572814B2
Source datasetuspto-grants-2009_08
ORD IDord-499f344b7fec4c908a5f68ec05031040
Source noteuspto-grants-2009_08