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HRID 279867作成日:2026年10月26日

2-Bromostyrene → Benzaldehyde, 2-ethenyl-

https://huagongshe.com/reaction/279867

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromostyreneHCID 16264—
反応物1-PiperidinecarboxaldehydeHCID 17429—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Benzaldehyde, 2-ethenyl-HCID 39391—

反応条件

温度-65 °C

反応手順

To a solution of 2-bromostyrene (115 mmol) in dry tetrahydrofuran (200 ml) at -65° C. under nitrogen was added dropwise n-butyllithium (115 mmol) in hexane. The reaction mixture was stirred at -65° C. for an additional hour and a solution of N-formylpiperidine (125 mmol) in tetrahydrofuran (50 ml) was added dropwise. The reaction mixture was allowed to warm to ambient temperature overnight. The reaction mixture was cooled to 0° C. and then quenched with saturated ammonium chloride (50 ml). The reaction mixture was extracted with diethyl ether (2×50 ml) and the combined organic phases were washed with 3N hydrochloric acid (2×50 ml), saturated aqueous sodium bicarbonate (50 ml), and brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to yield the Compound 2a which was directly used in the next reaction.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04587253
出典データセットuspto-grants-1986_05
ORD IDord-c1c226ff46244816b56974bf4ddc5953
出典メモuspto-grants-1986_05