戻る
化工社化工社 化学情報印刷レポート · 研究参考用
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

反応式

関与物質

役割名称HCID仕込み量
反応物3-(4-Chlorophenoxy)benzaldehydeHCID 616015—
反応物3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
溶媒IsopropanolHCID 3776—
生成物3-(3-(3-(4-Chlorophenoxy)benzylidene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine dihydrochlorideHCID 6733695274.1%

反応条件

温度80 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07662965B2
出典データセットuspto-grants-2010_02
ORD IDord-edab8f3343634601be0527e713a2acbf
出典メモuspto-grants-2010_02