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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258942생성일: 2026년 10월 26일

Butanal → Cinnamoylbenzene

https://huagongshe.com/reaction/258942

반응식

참여 물질

역할이름HCID투입량
반응물ButanalHCID 261—
반응물DimethylformamideHCID 6228—
반응물CinnamoylbenzeneHCID 7189—
반응물TriethylamineHCID 8471—
용매EthanolHCID 702—
생성물CinnamoylbenzeneHCID 7189—
생성물1,3-Diphenylheptane-1,4-dioneHCID 12288237—

반응 단계

Following the description in Example 1, 18 g (0.25 mol) of n-butyraldehyde, 52 g (0.25 mol) of benzylideneacetophenone and 500 ml of dimethylformamide, 250 ml of ethanol and 13.5 g (0.05 mol) of Cat. 1 are -- after addition of 10.1 g (0.1 mol) of triethylamine -- brought to the reflux temperature for 36 hours. To work up the batch, the solvent mixture is distilled off in a waterpump vacuum, the oily residue, when cold, is taken up in 250 ml of chloroform and the solution is washed successively with water, with dilute sodium bisulphite solution and twice more with water. The organic phase is separated off, the chloroform is distilled off and the residue is distilled in an oil pump vacuum. The fraction of boiling point0.2 = 140° - 170° C which is thus obtained is subsequently fractionated through a 30 cm Vigreux column. After a first running of benzylideneacetophenone, 1,3-diphenylheptane-1,4-dione is isolated as the main fraction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04035395
출처 데이터셋uspto-grants-1977_07
ORD IDord-351b6be7b1054901aad685f1af361849
출처 메모uspto-grants-1977_07