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HRID 223369作成日:2026年10月25日

Propyltriphenylphosphonium bromide → 1-Carbobenzoxy-4-(1-butylidene)piperidine

https://huagongshe.com/reaction/223369

反応式

関与物質

役割名称HCID仕込み量
反応物Propyltriphenylphosphonium bromideHCID 80374—
反応物Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-Carbobenzoxy-4-(1-butylidene)piperidineHCID 20522020—

反応手順

Butyl lithium (44 ml of 1.6 M in hexane) was added slowly to a stirred suspension of 27 g of (n-propyl)triphenylphosphonium bromide in 350 ml of tetrahydrofuran and the resulting solution was refluxed for 1 hour. The mixture was cooled in an ice bath and 18 g of N-carbobenzyloxy-4-piperidone was added. After stirring at room temperature of 0.5 hour, the solution was refluxed for 2 hours. The cooled mixture was concentrated under reduced pressure, partitioned between ether and water, and the ether layer was dried (sodium sulfate) and evaporated. The residue was filtered through silica gel with 20% ethyl acetate-hexane to give 10 g of 1-carbobenzoxy-4-(1-butylidene)piperidine as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04353901
出典データセットuspto-grants-1982_10
ORD IDord-f068b0d416624defa98b220467acb3f2
出典メモuspto-grants-1982_10