돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 573460생성일: 2026년 10월 27일

2,4-Dimethyl-3-cyclohexene carboxaldehyde → 1,3-Dioxane, 2-(2,4-dimethyl-3-cyclohexen-1-yl)-5-methyl-5-(1-methylpropyl)-

https://huagongshe.com/reaction/573460

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dimethyl-3-cyclohexene carboxaldehydeHCID 93375—
반응물1,3-Propanediol, 2-methyl-2-(1-methylpropyl)-HCID 98076—
생성물1,3-Dioxane, 2-(2,4-dimethyl-3-cyclohexen-1-yl)-5-methyl-5-(1-methylpropyl)-HCID 16070752—

반응 단계

An aqueous NaOH solution (30%, 420 g) was added at room temperature into a stirred mixture of 2,3-dimethyl pentanal (325 g, prepared as above in EXAMPLE II) and aqueous formaldehyde solution (CH2O) (30%, 722 g) while the reaction temperature was allowed to rise up to about 80° C. due to the exothermic reaction. After the addition was completed, the reaction mixture was cooled to about 40° C. The organic phases was separated and fractionally distilled to afford 2-sec-butyl-2-methyl-propane-1,3-diol (277 g). 2-sec-Butyl-2-methyl-propane-1,3-diol was reacted with 2,4-dimethyl-cyclohex-3-enecarbaldehyde to afford 5-sec-butyl-2-(2,4-dimethyl-cyclohex-3-enyl)-5-methyl-[1,3]dioxane according to previous disclosure (See, for example, U.S. Pat. No. 6,444,637).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029576B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-2dbb87e1e4a544c1baa0909fd54a0fea
출처 메모uspto-grants-2015_05