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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464488Generated: October 30, 2026

Potassium Hydroxide → 1,1-Dimethylethyl 4-ethenylphenyl carbonate

https://huagongshe.com/reaction/1464488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-Ethenylphenyl acetateHCID 75821—
ReactantDi-tert-butyl dicarbonateHCID 90495—
CatalystPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
Product1,1-Dimethylethyl 4-ethenylphenyl carbonateHCID 9348564%

Reaction Conditions

Temperature28 °C

Reaction Steps

A solution comprising 0.49 grams potassium hydroxide, 40 grams of 4-acetoxystyrene, and 100 grams of absolute ethanol was refluxed for 4 hours. The reaction solution was cooled to 28° C. and 13 grams of potassium hydroxide pellets were added over a period of 10 minutes. After an additional 30 minutes of reaction, 64 grams di-tertiary-butyl-dicarbonate was charged portionwise over 20 minutes and the reaction was stirred for an additional hour at 28° C. After aqueous washing, the reaction product was extracted with ethyl acetate. The ethyl acetate was stripped from the extraction mixture on a rotary evaporator and the residual oil was charged with 0.07 grams phenothiazine. Distillation at 0.1 Mm Hg gave 34.2 grams (64%) 4-tertiary-butoxycarbonyloxystyrene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304690
Source datasetuspto-grants-1994_04
ORD IDord-2e1ed0c5531a4b269cef5768c3b22de1
Source noteuspto-grants-1994_04