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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452355Generated: October 31, 2026

Trimethylsilyl iodide → 2,6-DI-Tert-butyl-4-hydroxyphenyl acetate

https://huagongshe.com/reaction/1452355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Acetoxy-3,5-di-tert-butylanisoleHCID 11821954—
SolventDichloromethaneHCID 6344—
Product2,6-DI-Tert-butyl-4-hydroxyphenyl acetateHCID 1113999880%

Reaction Steps

4-Acetoxy-3,5-di-tert-butylanisole (0.50 g) was dissolved in dichloromethane (2 ml). After cooling with ice, trimethylsilyl iodide (0.31 ml) was added dropwise. The mixture was allowed to warm slowly to room temperature and stirred for 2 days; thereafter, a saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture. The mixture was subjected to extraction with diethyl ether and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica Gel chromatography (15% ethyl acetate in n-hexane) to afford 4-acetoxy-3,5-di-tert-butylphenol [0.38 g (yield, 80%)] as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606089
Source datasetuspto-grants-1997_02
ORD IDord-3671c736d3bb4d8e902ce71db75abc1f
Source noteuspto-grants-1997_02