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HRID 466773생성일: 2026년 10월 24일

Cyclohexanone → 8-(2-Methyl-3-buten-2-ylperoxy)-p-menthane

https://huagongshe.com/ko/reaction/466773

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanoneHCID 7967—
반응물2,5-HexanedioneHCID 8035—
반응물CyclopentanoneHCID 8452—
반응물CyclododecanoneHCID 13246—
반응물3,3,5-TrimethylcyclohexanoneHCID 13398—
반응물Butyl levulinateHCID 16331—
반응물MethoxyacetoneHCID 22172—
용매AcetoneHCID 180—
용매Methyl Ethyl KetoneHCID 6569—
용매Ethyl ketoneHCID 7288—
용매Methyl Isobutyl KetoneHCID 7909—
생성물8-(2-Methyl-3-buten-2-ylperoxy)-p-menthaneHCID 19814568—

반응 단계

In the preparation of the present diperoxy ketals a t-alkenyl hydroperoxide (II) can be reacted in a usual way with a ketone in an acid medium. As examples of suitable ketones may be mentioned: acetone, methoxyacetone, methyl ethyl ketone, diethyl ketone, methyl isobutyl ketone, n-butyl-4-ketovalerate, 2,5-hexanedione, cyclohexanone, 3,3,5-trimethylcyclohexanone, cyclopentanone and cyclododecanone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05157087
출처 데이터셋uspto-grants-1992_10
ORD IDord-89e63318b7bd4baca3d4365ec665e90f
출처 메모uspto-grants-1992_10