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HRID 1678321作成日:2026年10月26日
5-Phenyl-2-furaldehyde → 3-(3-((5-Phenylfuran-2-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride
https://huagongshe.com/reaction/1678321
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 5-Phenyl-2-furaldehyde | HCID 2769420 | — |
| 反応物 | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 3-(3-((5-Phenylfuran-2-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride | HCID 67339451 | 181.8% |
反応手順
3-(5-Ammoniopentanoyl)pyridinium chloride (188 mg, 0.75 mmol) was transferred to a reaction vessel and treated with isopropanol (12 mL). 5-Phenyl-2-furaldehyde (193 mg, 1.12 mmol) was added, the reaction vessel was sealed, and the reaction was heated to 85° C. with stirring for 6 hours. The reaction was then cooled to room temperature, and the precipitate was recovered by vacuum filtration, washed with isopropanol and ether then dried under vacuum giving 264 mg (91%) of an orange solid. LC-MS: RT=5.15 min, [M+H]+=315.1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08008499B2 |
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| 出典データセット | uspto-grants-2011_08 |
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| ORD ID | ord-75ab2f627f15424ab020297c32ceee07 |
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| 出典メモ | uspto-grants-2011_08 |
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