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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638931Generated: November 1, 2026

Methyl iodide → 2-Methoxy-5-nitro-1-(prop-2-en-1-yl)-3-(trifluoromethoxy)benzene

https://huagongshe.com/reaction/638931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-Nitro-2-(prop-2-en-1-yl)-6-(trifluoromethoxy)phenolHCID 68686210—
Product2-Methoxy-5-nitro-1-(prop-2-en-1-yl)-3-(trifluoromethoxy)benzeneHCID 68683869—

Reaction Steps

1-Allyl-2-methoxy-5-nitro-3-trifluoromethoxybenzene was prepared from 2-allyl-4-nitro-6-trifluoromethoxyphenol and methyl iodide by following Method C. The reaction was conducted at room temperature for 17 h. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes (0-5%) as an eluent to give 1-allyl-2-methoxy-5-nitro-3-trifluoromethoxybenzene in 52% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691843B2
Source datasetuspto-grants-2010_04
ORD IDord-f9dbb15384af44aa8c804193e9c4f475
Source noteuspto-grants-2010_04