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HRID 128786作成日:2026年10月24日

Sodium Hydroxide → (2E)-2-Methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenol

https://huagongshe.com/ja/reaction/128786

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Sodium hydrideHCID 24758—
反応物Triethyl 2-phosphonopropionateHCID 107155—
反応物Sodium BicarbonateHCID 516892—
反応物5-(2,6,6-Trimethyl-1-cyclohexen-1-yl)pentanalHCID 19375154—
反応物DiisobutylaluminumhydrideHCID 21225700—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物(2E)-2-Methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenolHCID 1937503543.1%

反応手順

To a stirred solution of triethyl 2-phosphonopropionate (4.2 g) in THF (25 ml) under nitrogen is added sodium hydride (0.69 g of 60% dispersion in oil). After 30 minutes, 5-(2,6,6-trimethyl-1-cyclohexen-1-yl)pentanal (3.09 g) is added, and the mixture is stirred at reflux for16 hr. The reaction is cooled, poured into aqueous sodium bicarbonate, and extracted with ether. The extracts are concentrated and chromatographed with 30% dichloromethane in hexane to provide (2E)-2-methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenoic add ethyl ester as a colorless oil (2.4 g). This material (2.09 g) is reacted with diisobutylaluminum hydride (10 ml of 1.5M toluene solution) in toluene (20 ml) at -20° , stirred at 0° for 3 hr, then stirred for 16 hr with 1.0N sodium hydroxide solution. The mixture is extracted with ether, and the organic phase is concentrated and chromatographed with dichloromethane to provide 1.6 g of (2E)-2-methyl-7-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-heptenol as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464865
出典データセットuspto-grants-1995_11
ORD IDord-a201d8bc44424fc791242054bc5c15aa
出典メモuspto-grants-1995_11