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HRID 555974作成日:2026年10月27日

3-Phenylprop-2-Enal → alpha-Bromocinnamaldehyde

https://huagongshe.com/reaction/555974

反応式

関与物質

役割名称HCID仕込み量
反応物3-Phenylprop-2-EnalHCID 307—
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物BromineHCID 24408—
溶媒Acetic AcidHCID 176—
生成物alpha-BromocinnamaldehydeHCID 21585—

反応手順

1.33 g (10 mmol) cinnamaldehyde was dissolved in 5 mL glacial acetic acid and cooled on an ice-water bath. 1.62 g bromine was added, and anhydrous K2CO3 was then added, and it was stirred until no gas was evolving. After refluxing for 30 min, the reaction mixture was poured into 100 mL cold water with stirring, extracted with 50 mL ethyl ether three times. The combined ethyl ether layers were washed with water one time, saturated aqueous NaCl solution one time, dried over MgSO4 for 2 hours, filtrated, and the filtrate was dried under vacuum, and washed with anhydrous ethyl ether: petroleum ether (1:1) to give the title compound as light yellow powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08053577B2
出典データセットuspto-grants-2011_11
ORD IDord-33127781f18340369da56dfe4b8793c5
出典メモuspto-grants-2011_11