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HRID 127033作成日:2026年10月26日

3-Methyl-1-trichloromethyl-2-butenyl diazoacetate → 4-Trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane

https://huagongshe.com/reaction/127033

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-1-trichloromethyl-2-butenyl diazoacetateHCID 54224363—
触媒Bis(pentane-2,4-dione-kappa~2~O~2~,O~4~)copperHCID 45052134—
溶媒Diethyl EtherHCID 3283—
溶媒1,4-DioxaneHCID 31275—
生成物4-Trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexaneHCID 1252521856.5%

反応手順

To a refluxing solution of cupric acetylacetonate (0.07 g, 0.27 mole) in 70 ml of dioxane was added drop-dropwise over a 31/2 hour period, under an argon atmosphere, a solution of (±)-3-methyl-1-trichloromethyl-2-butenyl diazoacetate (1.09 g, 0.004 moles) and cupric acetylacetonate (0.007 g, 0.027 mmole) in 10 ml of dioxane. The reaction mixture was then heated under reflux for one hour and evaporated to dryness, yielding a residue which was dissolved in ether. The ethereal solution was washed successively with two portions of aqueous 1 N hydrochloric acid, two portions of aqueous sodium bicarbonate, and twice with saturated aqueous sodium chloride. After drying the solution over magnesium sulfate, the ether was evaporated to afford a pale yellow oil, which was purified by column chromatography on a silica gel column using a 9/1 mixture of n-hexane/ethyl acetate as the eluant, to give (±)-4-trichloromethyl-6,6-dimethyl-2-oxo-3-oxabicyclo[3.1.0]hexane (0.55 g, 53% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04254282
出典データセットuspto-grants-1981_03
ORD IDord-a24e740ee3754eeca22a32f79503d176
出典メモuspto-grants-1981_03