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HRID 980364作成日:2026年10月25日

Dicyclopropyl ketone → 4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran

https://huagongshe.com/reaction/980364

反応式

関与物質

役割名称HCID仕込み量
反応物Dicyclopropyl ketoneHCID 70721—
反応物Cyclopropanecarboxylic acid, 1-benzoyl-2-ethenyl-, ethyl esterHCID 11053884—
反応物Tricaprylylmethyl ammonium chlorideHCID 77620884—
生成物4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuranHCID 20191550—

反応手順

4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran was obtained in the usual manner by isomerizing ethyl 1-benzoyl-2-vinylcyclopropane-1-carboxylate. To catalyze the isomerization, tricaprylylmethylammonium chloride was employed at a 20 percent weight level. The mixture was heated at 150° C. for about two hours after which time only about 7 percent of the cyclopropyl ketone remained. After two distillations, essentially pure 4-carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran was obtained. The product (B.P. 110° C. @ 0.1 mm Hg: nD25° 1.5570) had a pleasing aroma that was somewhat coumarin-like in odor character. Nuclear magnetic resonance and infrared spectroscopic analysis confirmed the structure ##STR16##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04636571
出典データセットuspto-grants-1987_01
ORD IDord-7f17823642fb467e87bf58ec7cbf680b
出典メモuspto-grants-1987_01