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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 389177Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/389177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Penten-1-OLHCID 13181—
EduktSodium HydroxideHCID 14798—
EduktDiisopropylethylamineHCID 81531—
EduktTriphosgeneHCID 94429—
EduktHCID 59493566HCID 59493566—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktEthyl (2S)-2-{[(pent-4-en-1-yloxy)carbonyl]amino}non-8-enoateHCID 86647499122,3%

Reaktionsschritte

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].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08377874B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-9b3472f1b54542038d9f5857c636b3fe
Quellennotizuspto-grants-2013_02