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HRID 258942作成日:2026年10月26日

Butanal → Cinnamoylbenzene

https://huagongshe.com/reaction/258942

反応式

関与物質

役割名称HCID仕込み量
反応物ButanalHCID 261—
反応物DimethylformamideHCID 6228—
反応物CinnamoylbenzeneHCID 7189—
反応物TriethylamineHCID 8471—
溶媒EthanolHCID 702—
生成物CinnamoylbenzeneHCID 7189—
生成物1,3-Diphenylheptane-1,4-dioneHCID 12288237—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04035395
出典データセットuspto-grants-1977_07
ORD IDord-351b6be7b1054901aad685f1af361849
出典メモuspto-grants-1977_07