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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264707Generated: October 31, 2026

Methyl iodide → HCID 57675751, compound

https://huagongshe.com/reaction/2264707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 57675741HCID 57675741—
CatalystHCID 178418778HCID 178418778—
SolventAcetonitrileHCID 6342—
ProductHCID 57675751HCID 5767575177%

Reaction Conditions

Temperature40 °C

Reaction Steps

[1-(4-Benzyloxyphenyl)-5-methoxy-1H-indol-2-yl]methanol (0.2 g, 0.56 mmol) was dissolved in acetonitrile (2 mL), and iodomethane (0.35 mL, 5.6 mmol) and silver(I) oxide (0.39 g, 1.68 mmol) were added. The mixture was stirred overnight at 40° C., then cooled to room temperature and filtered through a pad of Celite. The filtrate was concentrated. SiO2 chromatography with 3-50% ethyl acetate/hexanes gave 0.16 g (77% yield) of the desired product. LC-MS (C24H23NO3 calc'd 373) m/z 374 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855224B2
Source datasetuspto-grants-2010_12
ORD IDord-5d534edf7d8d487cb69c25cd405da09d
Source noteuspto-grants-2010_12