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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52398생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 8-t-Butyl-2-(4,6-dimethylpyrimid-2-ylaminomethyl)-1,4-dioxaspiro(4,5)decane

https://huagongshe.com/ko/reaction/52398

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-tert-ButylcyclohexanoneHCID 7392—
반응물3-(4,6-Dimethylpyrimid-2-ylamino)propane-1,2-diolHCID 19963666—
용매BenzeneHCID 241—
생성물8-t-Butyl-2-(4,6-dimethylpyrimid-2-ylaminomethyl)-1,4-dioxaspiro(4,5)decaneHCID 1996366790%

반응 단계

3-(4,6-dimethylpyrimid-2-ylamino)-propane-1,2-diol (4.0 g, 20 mmol), 4-t-butyl cyclohexanone (3.08 g, 20 mmol) and p-toluenesulfonic acid (4.3 g, 22 mmol) in 50 ml benzene were refluxed on a water trap for 1 hour. The reaction mixture was washed twice with saturated aqueous sodium carbonate (50 ml), dried with magnesium sulphate and evaporated in vacuum. Kugelrohr- distillation of the resulting oil yielded 6.0 g of a colourless oil (b.p. 200° C./0.2 mbar) which was recrystallised from light petroleum to yield 5.0 g of colourless crystals (m.p. 121°-124° C.). GLG-MS analysis indicates an approximately 1:1 mixture of diastereoisomers (cis/trans).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616708
출처 데이터셋uspto-grants-1997_04
ORD IDord-ea9d841dea47442f9ffde8a62db28f90
출처 메모uspto-grants-1997_04