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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830809Generated: October 30, 2026

Methyl iodide → HCID 22048482, compound

https://huagongshe.com/reaction/1830809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 22048484HCID 22048484—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 22048482HCID 22048482—

Reaction Steps

A mixture of intermediate (21) (0.0132 mol), iodomethane (0.0264 mol) and benzyltriethylammonium chloride (0.00132 mol) in THF (50 ml) and sodium hydroxide 10N (50 ml) was stirred at room temperature overnight. EtOAc was added. The mixture was decanted. The organic layer was dried, filtered and the solvent was evaporated. The residue (2.9 g) was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 95/5/0.1; 15–40 μm). The pure fractions were collected and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: toluene/2-propanol/NH4OH 70/29/1; 15–40 μm). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from diethyl ether. The precipitate was filtered off and dried, yielding 0.45 g of 4-(3-chlorophenyl)-6-[hydroxy(1-methyl-1H-imidazol-5-yl)methyl]-1-methyl-2(1H)-quinolinone, mp. 167° C. (intermediate 22).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067531B2
Source datasetuspto-grants-2006_06
ORD IDord-d982624099d148adb1dd48dd5c89943d
Source noteuspto-grants-2006_06