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HRID 1444745作成日:2026年10月27日
3-(4-Chlorophenoxy)benzaldehyde → 3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride
https://huagongshe.com/reaction/1444745
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-(4-Chlorophenoxy)benzaldehyde | HCID 616015 | — |
| 反応物 | 3-(5-Ammoniopentanoyl)pyridinium chloride | HCID 67337657 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochloride | HCID 67336952 | 74.1% |
反応手順
3-(5-Ammoniopentanoyl)pyridinium chloride (162 mg, 0.64 mmol) was suspended in a reaction vessel with i-propanol (12 mL). 3-(4-chlorophenoxy)benzaldehyde (225 mg, 0.97 mmol) was then added and the reaction vessel sealed. The reaction was heated to 80° C. overnight and then cooled to room temperature. The precipitate was recovered by vacuum filtration, washed with a 20% i-propanol in hexane solution then dried under vacuum giving 161 mg (56%) of a tan-colored solid. LC-MS: RT=6.22 min, [M+H]+=375.1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07662965B2 |
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| 出典データセット | uspto-grants-2010_02 |
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| ORD ID | ord-edab8f3343634601be0527e713a2acbf |
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| 出典メモ | uspto-grants-2010_02 |
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