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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913989Generated: October 31, 2026

Potassium Hydroxide → Propaneperoxoic acid, 2,2-dimethyl-, 1,1-dimethylpropyl ester

https://huagongshe.com/reaction/1913989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
ReactantPivaloyl chlorideHCID 62493—
Reactanttert-Amyl hydroperoxideHCID 76962—
SolventWaterHCID 962—
ProductPropaneperoxoic acid, 2,2-dimethyl-, 1,1-dimethylpropyl esterHCID 121798—

Reaction Steps

The reaction is effected in a reactor arrangement of a first reactor of type D with two reactors of type B connected downstream in series. 0.26 kg/l·h of an 88% by weight solution of tert-amyl hydroperoxide in water, 0.47 kg/l·h of a 25% by weight solution of potassium hydroxide in water, 0.50 kg/l·h of a 25% by weight solution of sodium hydroxide in water and 0.26 kg/l·h of pivaloyl chloride are fed to the first reactor. The metering rates are based on the total volume of the reactor arrangement in litres. Cooling with cooling water keeps the internal temperature in the first reactor at 25° C. and in the two downstream reactors at 15° C. The reaction mixture withdrawn from the third reactor is mixed with 0.79 kg/l·h of demineralized water and 0.08 kg/l·h of isododecane, and the organic phase is removed. The organic phase is washed successively with an 8% by weight solution of sodium hydroxide in water, with a solution of 10% by weight of sodium sulphite in water comprising acetic acid and with demineralized, water, and then dried with calcium chloride. 0.42 kg/l·h of a 75% by weight solution of tert-amyl peroxypivalate in isododecane is obtained (80.6% based on pivaloyl chloride).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609883B2
Source datasetuspto-grants-2013_12
ORD IDord-78dbe773a7634f789f46aaedda0d0209
Source noteuspto-grants-2013_12