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HRID 389177作成日:2026年10月27日

4-Penten-1-OL → Ethyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoate

https://huagongshe.com/reaction/389177

反応式

関与物質

役割名称HCID仕込み量
反応物4-Penten-1-OLHCID 13181—
反応物Sodium HydroxideHCID 14798—
反応物DiisopropylethylamineHCID 81531—
反応物TriphosgeneHCID 94429—
反応物ethyl (2S)-2-aminonon-8-enoateHCID 59493566—
溶媒1,4-DioxaneHCID 31275—
生成物Ethyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoateHCID 86647499122.3%

反応手順

To a stirred solution of pent-4-en-1-ol (0.62 g, 7.21 mmol) and DIPEA (1.26 mL, 7.21 mmol) in anhydrous 1,4-dioxane (20 ml), at 10° C. and under nitrogen, was slowly added a solution of triphosgene (0.75 g, 2.52 mmol) in anhydrous 1,4-dioxane (20 mL). The reaction mixture was stirred at RT for 1 hour, and ethyl (2S)-2-aminonon-8-enoate*HCl (0.85 g, 3.61 mmol) and 1 M aqueous NaOH (7.21 ml, 7.21 mmol) added, and the reaction mixture was heated to 50° C. for 15 hours. After cooling to RT, the reaction mixture was basified to pH 8 with 1M aqueous NaOH and extracted with ether (3×200 ml). The combined organic phases were washed with water (100 mL), brine (50 mL), dried over Na2SO4, filtered and concentrated. The residue was chromatographed on silica gel (5 to 75% EtOAc in hexane) to give the title compound (0.96 g). LRMS (ESI) m/z 312.5 [(M+H)+; calcd for C17H30NO4: 312.2].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08377874B2
出典データセットuspto-grants-2013_02
ORD IDord-9b3472f1b54542038d9f5857c636b3fe
出典メモuspto-grants-2013_02