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HRID 856115作成日:2026年10月24日

2-Pentanone, 5-(acetyloxy)- → 4-Methyl-4-pentenyl acetate

https://huagongshe.com/ja/reaction/856115

反応式

関与物質

役割名称HCID仕込み量
反応物2-Pentanone, 5-(acetyloxy)-HCID 21258—
反応物Potassium tert-butoxideHCID 23665647—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒TetrahydrofuranHCID 8028—
生成物4-Methyl-4-pentenyl acetateHCID 1223138560.4%

反応手順

Potassium tert-butoxide (9.4 g, 84 mmol) was added to a mixture of methyltriphenylphosphonium bromide (30 g, 84 mmol) in THF (300 ml), and the mixture was stirred at room temperature for 40 minutes. To the mixture a solution of 4-oxopentyl acetate (9.9 g, 68.8 mmol) in THF (30 ml) was gradually added dropwise while cooling in an ice-bath, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into ice water, and extracted with diethyl ether twice. The extracts were combined, washed with brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=4/1) to afford 4-methyl-4-pentenyl acetate (5.9 g, yield 60.4%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07262212B2
出典データセットuspto-grants-2007_08
ORD IDord-20fd1cb0da5b437da272849fb0179b44
出典メモuspto-grants-2007_08