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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322981Generated: October 27, 2026

Methyl iodide → 2-(5-Methoxy-2-methylphenyl)-[1,3]dioxolane

https://huagongshe.com/reaction/322981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,3-Dioxolane, 2-(2-bromo-5-methoxyphenyl)-HCID 11184503—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Methoxy-2-methylphenyl)-[1,3]dioxolaneHCID 22171233—

Reaction Conditions

Temperature-65 °C

Reaction Steps

A stirred solution of 2-(2-bromo-5-methoxyphenyl)-[1,3]dioxolane (25.92 g) in tetrahydrofuran (400 mL) at −70° C. is treated dropwise with a solution of n-butyl lithium in hexanes (48.0 mL, 2.5 M). After stirring for 10 minutes methyl iodide (21.29 g) is added dropwise whilst maintaining the temperature at −65° C. The reaction mixture is stirred at −65° C. for 1 hour, allowed to warm to room temperature and stirring is continued for a further hour. The reaction mixture is evaporated and the residue partitioned between ethyl acetate (50 mL) and water (50 mL). The organic phase is washed with brine (500 mL),dried over magnesium sulphate and evaporated to give 2-(5-methoxy-2-methyl-phenyl)-[1,3]dioxolane (18.25 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211234B1
Source datasetuspto-grants-2001_04
ORD IDord-82e3fcedf4dd42e0803a1b9eea3c4cc5
Source noteuspto-grants-2001_04