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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925688Generated: October 28, 2026

Methyl iodide → 1-tert-butyl-3-methoxybenzene

https://huagongshe.com/reaction/1925688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPhenol, 3-(1,1-dimethylethyl)-HCID 11450—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-tert-butyl-3-methoxybenzeneHCID 5325968113.2%

Reaction Steps

To a solution of 3-tert-butylphenol (5.0 g; 33.28 mmol) in N,N-dimethylformamide (166 mL) at room temperature under nitrogen was added sodium hydride (2.0 g; 49.92 mmol). The reaction mixture was stirred at room temperature for 10 minutes and then iodomethane (6.2 mL; 99.84 mmol) was added. After stirring at room temperature overnight, the reaction mixture was quenched with water and aqueous hydrochloric acid (2N) and extracted with ethyl acetate. The combined organic phases were successively washed with water and aqueous saturated sodium chloride, dried over magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the resulting crude residue was purified by automated silica gel column chromatography (Biotage®) eluting with ethyl acetate/hexanes (0 to 40% v/v over 400 mL gradient elution) to yield the title product as a clear oil (6.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178699B2
Source datasetuspto-grants-2012_05
ORD IDord-f836bcf7d034451993820f468b25ab4d
Source noteuspto-grants-2012_05