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HRID 1968969作成日:2026年10月25日

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

https://huagongshe.com/reaction/1968969

反応式

関与物質

役割名称HCID仕込み量
反応物Isobutyl MethacrylateHCID 7352—
反応物2-(Trimethylsiloxy)-1,3-butadieneHCID 554657—
反応物1-Butyl-3-methylimidazolium hexafluorophosphateHCID 2734174—
触媒4,4'-Methylenebis(2,6-di-tert-butylphenol)HCID 8372—
生成物2-Methylpropyl 1-methyl-4-oxocyclohexanecarboxylateHCID 5944413221.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08426443B2
出典データセットuspto-grants-2013_04
ORD IDord-4bc67d6646e94da494adc0ead9ce65d5
出典メモuspto-grants-2013_04