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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900498Generated: October 29, 2026

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

https://huagongshe.com/reaction/1900498

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 numberUS05574178
Source datasetuspto-grants-1996_11
ORD IDord-76f62dfe60f74e48881eae31ffc232e2
Source noteuspto-grants-1996_11