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HRID 73534作成日:2026年10月25日

Sodium Bicarbonate → (S)-benzyl 3-(tert-butoxycarbonylamino)-5-ethylidenepiperidine-1-carboxylate

https://huagongshe.com/reaction/73534

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物Potassium tert-butoxideHCID 23665647—
反応物HCID 68922849HCID 68922849—
触媒Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-benzyl 3-(tert-butoxycarbonylamino)-5-ethylidenepiperidine-1-carboxylateHCID 68922866—

反応条件

温度0 °C

反応手順

To a suspension of ethyltriphenylphosphonium bromide (11 eq) in 14 mL of THF was added potassium tert-butoxide (10 eq) at room temperature. The reaction mixture was stirred at that temperature for 20 minutes. Then the reaction was cooled to 0° C., and (S)-benzyl 3-(tert-butoxycarbonylamino)-5-oxopiperidine-1-carboxylate (1 eq) in 7 mL of THF was added to the reaction mixture. The reaction was allowed to warm up room temperature. After being stirred for 40 minutes, the reaction mixture was poured into aq. sodium bicarbonate and extracted with ethyl acetate. The organic layer was separated and washed with brine, then dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The crude residue was purified by flash chromatography (EtOAc:hexanes=2:1) to yield (S)-benzyl 3-(tert-butoxycarbonylamino)-5-ethylidenepiperidine-1-carboxylate. LC/MS (m/z): 261.2 (MH+-100), Rt:1.12 min. HPLC: Rt:4.31 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829193B2
出典データセットuspto-grants-2014_09
ORD IDord-e6f8476ce6314680b863fca27c4338a2
出典メモuspto-grants-2014_09