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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9627Generated: October 26, 2026

Potassium Iodide → Ethyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoate

https://huagongshe.com/reaction/9627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantEthyl 2-(4-acetyl-2-methylphenoxy)-2-methylpropanoateHCID 16756777—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-[4-(acetyloxy)-2-methylphenoxy]-2-methylpropanoateHCID 21986549—

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of ethyl 2-(4-acetyl-2-methylphenoxy)-2-methylpropanoate (intermediate 8, 37.33 g) in dichloromethane (650 ml) was treated with 4-toluenesulphonic acid (2.75 g) followed by m-chloroperbenzoic acid (60.5 g) and the mixture warmed to 40° C. and stirred under nitrogen for 19 hours. The cooled mixture was treated with dichloromethane (350 ml) and the resulting mixture added to aqueous potassium iodide (1000 ml, 10% solution). The organic layer was collected and washed twice with water and brine, then dried over sodium sulfate, filtered and the filtrate concentrated to give the title compound as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091237B2
Source datasetuspto-grants-2006_08
ORD IDord-ac4f6997785540cfabd1e40607d0df66
Source noteuspto-grants-2006_08