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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1071767생성일: 2026년 10월 27일

Benzaldehyde → 2-Benzylidene-1,3-indandione

https://huagongshe.com/reaction/1071767

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물1,2-IndandioneHCID 123358—
반응물Boron monoxideHCID 6327189—
촉매PiperidineHCID 8082—
용매BenzeneHCID 241—
생성물2-Benzylidene-1,3-indandioneHCID 237822—

반응 단계

(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, 2 H), 8.06-7.99 (m, 2 H), 7.90 (s, 1 H), 7.84-7.79 (m, 2 H), 7.58-7.50 (m, 3 H); 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06906105B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-1a7df1ec91ff4c14866d69c7210e6156
출처 메모uspto-grants-2005_06