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HRID 8744作成日:2026年10月23日

1-Pentene, 5-bromo- → Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate

https://huagongshe.com/ja/reaction/8744

反応式

関与物質

役割名称HCID仕込み量
反応物1-Pentene, 5-bromo-HCID 70704—
反応物1-N-Boc-4-Piperidinecarboxylic acid methyl esterHCID 392870—
反応物Sodium BicarbonateHCID 516892—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-(pent-4-en-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylateHCID 1123218199.2%

反応手順

To a solution of potassium bis(trimethylsilyl)amide (30.7 g, 0.15 mol) in tetrahydrofuran (750 mL) at 0° C. was added a solution of methyl 1-(tert-butoxycarbonyl)piperidine-4-carboxylate (25 g, 0.10 mol) from Step A in tetrahydrofuran (250 mL) and the reaction mixture was stirred for 1 h. 5-Bromo-1-pentene (19.4 mL, 0.164 mol) was added and the reaction mixture was allowed to warm to room temperature for 1.5 h. The reaction mixture was then poured into saturated sodium bicarbonate solution and extracted three times with ethyl acetate. The organic layers were combined and washed with brine, dried over sodium sulfate, filtered, and concentrated to afford the title compound (30.9 g) which was used in the next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091211B2
出典データセットuspto-grants-2006_08
ORD IDord-292d55b0aa854c219dbd269febe9a838
出典メモuspto-grants-2006_08