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Dicyclopropyl ketone → 4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dicyclopropyl ketone | HCID 70721 | — |
| 反応物 | Cyclopropanecarboxylic acid, 1-benzoyl-2-ethenyl-, ethyl ester | HCID 11053884 | — |
| 反応物 | Tricaprylylmethyl ammonium chloride | HCID 77620884 | — |
| 生成物 | 4-Carbethoxy-5-phenyl-2-vinyl-2,3-dihydrofuran | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04636571 |
| 出典データセット | uspto-grants-1987_01 |
| ORD ID | ord-7f17823642fb467e87bf58ec7cbf680b |
| 出典メモ | uspto-grants-1987_01 |