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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195278Generated: November 3, 2026

Methanol → 5-(2-Benzyloxyethyl)-6-methyl-1,3-benzodioxole

https://huagongshe.com/reaction/1195278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl iodideHCID 6328—
ReactantHCID 19001633HCID 19001633—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product5-(2-Benzyloxyethyl)-6-methyl-1,3-benzodioxoleHCID 19001663—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3.0 g of 5-(2-benzyloxyethyl)-6-bromo-1,3-benzodioxole was dissolved in 100 m(of anhydrous ether. 8.5 ml of a 1.6 M solution of n-butyllithium in hexane was added to the solution at -78° C. and the reaction was conducted at -50° C. for 2 h. The reaction mixture was cooled again to -78° C. 6.4 g of methyl iodide was added thereto and the temperature was gradually elevated to room temperature. Methanol and water were added to the reaction mixture. After extraction with ethyl acetate, the extract was dried over magnesium sulfate and concentrated under reduced pressure to obtain a crude methyl compound. After purification according to silica gel column chromatography (ethyl acetate/ hexane=2:98), 1.9 g of the intended compound was obtained in the form of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110956
Source datasetuspto-grants-1992_05
ORD IDord-cff42e49f36945b790603d9208912868
Source noteuspto-grants-1992_05