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HRID 47307作成日:2026年10月25日

Bromide ion → Benzyl 4-methylidenepiperidine-1-carboxylate

https://huagongshe.com/reaction/47307

反応式

関与物質

役割名称HCID仕込み量
反応物Bromide ionHCID 259—
反応物Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
反応物HCID 178418922HCID 178418922—
溶媒TetrahydrofuranHCID 8028—
生成物Benzyl 4-methylidenepiperidine-1-carboxylateHCID 15519136159.7%

反応手順

51.1 g of methyltoluphenylphosphonium bromide was added to a mixture of 16.1 g tert-butoxy potassium and 500 ml tetrahydrofuran, and then stirred for 1 hr and 20 min at room temperature. 16.1 g of benzyl 4-oxo-1-piperidinecarboxylate was added thereto, and the mixture was stirred for 2 hr and 40 min at room temperature. The reaction solution was evaporated, diethyl ether was added thereto, and then filtered through Celite. The filtrate was washed with water and brine, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was evaporated, and the resulting residue was subjected to silica gel-column chromatography to give 25.5 g of benzyl 4-methylene-1-piperidinecarboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699870B2
出典データセットuspto-grants-2004_03
ORD IDord-28f15de1c3324835b374d20f7606c6c9
出典メモuspto-grants-2004_03