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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 909411생성일: 2026년 10월 27일

Hydrochloric Acid → tert-BUTYL PEROXYPIVALATE

https://huagongshe.com/reaction/909411

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물tert-Butyl hydroperoxideHCID 6410—
반응물Potassium HydroxideHCID 14797—
반응물2-MethylundecaneHCID 23459—
반응물Pivaloyl chlorideHCID 62493—
용매WaterHCID 962—
생성물tert-BUTYL PEROXYPIVALATEHCID 6123893.7%

반응 단계

Before the start of the reaction, the loop reactor is filled with a solution of 26.0% by weight of tert-butyl hydroperoxide and 16.2% by weight of potassium hydroxide in water. Initially 26.0 kg/h of a solution of 70% by weight of tert-butyl hydroperoxide in water, 25.0 kg/h of a solution of 45% by weight of potassium hydroxide in water, 26.4 kg/h of water and 18.0 kg/h of pivaloyl chloride are then fed to the loop reactor. Cooling with cooling water keeps the internal temperature at 15° C. in the loop reactor and at 10° C. in the stirred cell reactor. The partial neutralization is effected with 6.0 kg/h of 31% by weight hydrochloric acid with addition of 8.2 kg/h of isododecane at a temperature of 8° C. The organic phase is extracted with 33.2 kg/h of a 20% by weight aqueous solution of potassium hydroxide. This affords 37.4 kg/h of aqueous extract comprising 11.6% by weight of tert-butyl hydroperoxide and 17.6% by weight of potassium hydroxide, which are feeded into the loop reactor. From the time at which aqueous extract is recycled into the loop reactor, the metered addition of the feedstocks is changed to 19.8 kg/h of a solution of 70% by weight of tert-butyl hydroperoxide in water, 10.2 kg/h of a solution of 45% by weight of potassium hydroxide in water and 9.8 kg/h of water. After the extraction, the organic phase is washed with 36.0 kg/h of a solution of 1% by weight of sodium sulphite and 0.2% by weight of sulphuric acid, and dried by stripping at 20° C. and 45 mbar. 32.4 kg/h of a 75.3% by weight solution of tert-butyl peroxypivalate in isododecane are obtained (93.7% yield based on pivaloyl chloride).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017801B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-f6f1ea73cac64289a16a7126986ae66b
출처 메모uspto-grants-2011_09