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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71476Generated: October 26, 2026

Methyl iodide → 2-Methoxy-1,3-dimethyl-5-nitrobenzene

https://huagongshe.com/reaction/71476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Xylenol, 4-nitro-HCID 17030—
ReactantN2,N4-bis(3-methoxy-4-methoxycarbonylphenyl)-5-fluoro-2,4-pyrimidinediamineHCID 22060643—
Product2-Methoxy-1,3-dimethyl-5-nitrobenzeneHCID 139835—

Reaction Steps

In a manner analogous to the preparation of N2,N4-bis[3-methoxy-4-(methoxycarbonyl)phenyl]-5-fluoro-2,4-pyrimidinediamine, the reaction of 2,6-dimethyl-4-nitrophenol (1.67 g, 10 mmol), potassium carbonate (13 g, 0.1 mol) and iodomethane (2.5 mL, 50 mmol) gave 2,6-dimethyl-1-methoxy-4-nitrobenzene. Hydrogenation of 2,6-dimethyl-1-methoxy-4-nitrobenzene gave 3,5-dimethyl-4-methoxyaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822685B2
Source datasetuspto-grants-2014_09
ORD IDord-ed81eb9318624099ac7948398a4867e9
Source noteuspto-grants-2014_09