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HRID 1968969생성일: 2026년 10월 25일

Isobutyl Methacrylate → 2-Methylpropyl 1-methyl-4-oxocyclohexanecarboxylate

https://huagongshe.com/reaction/1968969

반응식

참여 물질

역할이름HCID투입량
반응물Isobutyl MethacrylateHCID 7352—
반응물2-(Trimethylsiloxy)-1,3-butadieneHCID 554657—
반응물1-Butyl-3-methylimidazolium hexafluorophosphateHCID 2734174—
촉매4,4'-Methylenebis(2,6-di-tert-butylphenol)HCID 8372—
생성물2-Methylpropyl 1-methyl-4-oxocyclohexanecarboxylateHCID 5944413221.4%

반응 단계

2-(Trimethylsilyloxy)buta-1,3-diene (40 g, 281 mmol) was weighed into a Teflon™ microwave container. Isobutyl methacrylate (50.8 mL, 317 mmol) was added followed by 4,4′-methylenebis(2,6-di-tert-butylphenol) (0.5 g, 1.177 mmol), finally 1-butyl-3-methylimidazolium hexafluorophosphate (0.5 mL) was added, the vessel transferred to the Advancer microwave and heated for 4 hr (normal absorption, no fixed hold time, 190° C.). After 1 hr 20 min an error message was seen for the temperature probe, the error was cleared and heating was continued for a further hour. At this time the software had frozen forcing a shutdown at the mains. The reaction mixture was allowed to cool to RT. Tetrahydrofuran (THF) (200 mL) was added and the solution transferred to a round bottomed flask. 2M HCl was added and the reaction mixture left to stir overnight. DCM was added to the reaction mixture, whereupon an emulsion formed. An attempt to filter this was unsuccessful, and the mixture was left to stand overnight. The organic layer was separated, dried (Na2SO4) and evaporated to give a sticky oil. Flash column chromatography, eluting with ethyl acetate/isohexane gave 2-methylpropyl 1-methyl-4-oxocyclohexanecarboxylate as a yellow oil (12.74 g, 60.0 mmol, 21.35% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08426443B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-4bc67d6646e94da494adc0ead9ce65d5
출처 메모uspto-grants-2013_04