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HRID 66165作成日:2026年10月26日
Ethanone, 2-(2-imidazolidinylidene)-1-phenyl- → 2-(2-Ethoxy-2-phenyl-ethenyl)-2-imidazoline tetrafluoroborate
https://huagongshe.com/reaction/66165
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ethanone, 2-(2-imidazolidinylidene)-1-phenyl- | HCID 821546 | — |
| 反応物 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(2-Ethoxy-2-phenyl-ethenyl)-2-imidazoline tetrafluoroborate | HCID 86736218 | — |
反応手順
20 g (0.105 mole) of triethyloxonium-tetrafluoroborate is dissolved in 200 ml of methylene chloride. To the solution is added 18.8 g (0.1 mole) of crystalline 2-(2-imidazolidinylidene)-acetophenone [m.p. 211°-212°, see J. Klosa, Arch.Pharmaz. 286, 397 (1953)]. After the slightly exothermic reaction has subsided, the reaction mixture, a clear yellow solution, is stirred for 16 hours at room temperature; it is subsequently concentrated to dryness in the rotary evaporator; and the crystallising residue is suspended in 300 ml of ethyl acetate. The suspension is cooled to 5°, and the crystals are filtered off with suction to obtain 2-(2-ethoxy-2-phenyl-ethenyl)-2-imidazoline-tetrafluoroborate, m.p. 151°-152°. After drying at 60° in vacuo, the product is further employed without additional purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04130652 |
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| 出典データセット | uspto-grants-1978_12 |
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| ORD ID | ord-7949cbad5ce44b3bb410b158ea87f323 |
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| 出典メモ | uspto-grants-1978_12 |
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