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HRID 990897作成日:2026年10月26日

Benzaldehyde → 2-Benzylidene-1,3-indandione

https://huagongshe.com/reaction/990897

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物1,2-IndandioneHCID 123358—
反応物Boron monoxideHCID 6327189—
触媒PiperidineHCID 8082—
溶媒BenzeneHCID 241—
生成物2-Benzylidene-1,3-indandioneHCID 237822—

反応手順

(8) (Chem. Pharm. Bull. 1974, 22(2), 448-451). Boron oxide (720 mg, 10.26 mmol) and benzaldehyde (800 mg, 7.53 mmol) were added to a stirred solution of the indandione (1.00 g, 6.84 mmol) and piperidine (3 drops) in 10.2 ml of benzene. The solution was refluxed with stirring for 30 minutes. After filtration of the solution, the filtrate was concentrated under reduced pressure. The resulting crystalline solid was recrystallized from ethanol to afford 1.00 g (62.4%) of yellowish-green platelets: mp 149.5-150.0° C. (lit. mp 150° C., Okukawa, et al., Chem. Pharm. Bull., 1974, 22(2), 448-451). 1H NMR (250 MHz) δ 8.47-8.45 (m, 2H), 8.06-7.99 (m, 2H), 7.90 (s, 1H), 7.84-7.79 (m, 2H), 7.58-7.50 (m, 3H); 13C NMR (62.7 MHz) 190.5, 189.2, 147.2, 142.7, 140.2, 135.6, 135.4, 134.3, 133.4, 133.2, 129.3, 129.0, 123.5, 123.5 ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06462075B1
出典データセットuspto-grants-2002_10
ORD IDord-7cb3bddf1d62412c8322c6bc556bc9ef
出典メモuspto-grants-2002_10