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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167333Generated: October 27, 2026

Methyl iodide → 2,4-Dimethoxy-5-methoxymethyl-benzonitrile

https://huagongshe.com/reaction/1167333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant5-Hydroxymethyl-2,4-dimethoxy-benzonitrileHCID 22996245—
SolventTetrahydrofuranHCID 8028—
Product2,4-Dimethoxy-5-methoxymethyl-benzonitrileHCID 2299618895%

Reaction Steps

To a solution of 5-hydroxymethyl-2,4-dimethoxy-benzonitrile (218 mg, 1.128 mmol) in tetrahydrofuran (10 mL) cooled to 0° C. were sequentially added sodium hydride (34.2 mg, 1.354 mmol) and iodomethane (140 μL, 2.256 mmol). The icebath was removed after 5 min and the reaction mixture was stirred at room temperature under argon for 12 h. Water was added and the product was extracted with methylene chloride (2×15 mL). The organic layers were washed with brine (1×2 mL) and dried over anhydrous sodium sulfate. The solid was filtered off and the filtrate was concentrated in vacuo. Purification of the crude residue by flash chromatography (Biotage system, KP-Sil™ 32-63 μm, 60 Å silica gel) eluting with 40% ethyl acetate in hexanes yielded 2,4-dimethoxy-5-methoxymethyl-benzonitrile as a white solid (221 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617346B1
Source datasetuspto-grants-2003_09
ORD IDord-3c1a480ddc8b4c1aa4f3df9902060f06
Source noteuspto-grants-2003_09