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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913992Generated: November 1, 2026

tert-Butyl hydroperoxide → Propaneperoxoic acid, 2-methyl-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/1913992

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantPotassium HydroxideHCID 14797—
ReactantIsobutyryl chlorideHCID 62325—
SolventWaterHCID 962—
ProductPropaneperoxoic acid, 2-methyl-, 1,1-dimethylethyl esterHCID 61023—

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. 1.22 kg/l·h of a 26% by weight solution of tert-butyl hydroperoxide and 17% by weight of potassium hydroxide in water and 0.32 kg/l·h of isobutyroyl 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internal temperature in the first reactor at 26° C. and in the two downstream reactors at 20° C. The reaction mixture withdrawn from the third reactor is mixed with 0.79 kg/l·h of demineralized water and 0.14 kg/l·h of isododecane, and the organic phase is removed.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. 0.54 kg/l·h of a 75% by weight solution of tert-butyl peroxyisobutyrate in isododecane is obtained (86.0% based on isobutyroyl chloride).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609883B2
Source datasetuspto-grants-2013_12
ORD IDord-dec9501fbb9a49e4bb2a9b739b7c0397
Source noteuspto-grants-2013_12