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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 388220Erstellt: 26. Oktober 2026

4-Penten-1-OL → 3-Methyl-N-{[(pent-4-en-1-yl)oxy]carbonyl}-L-valine

https://huagongshe.com/reaction/388220

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Penten-1-OLHCID 13181—
EduktSodium HydroxideHCID 14798—
EduktDiisopropylethylamineHCID 81531—
EduktTriphosgeneHCID 94429—
EduktL-tert-LeucineHCID 164608—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt3-Methyl-N-{[(pent-4-en-1-yl)oxy]carbonyl}-L-valineHCID 45379928147,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Diisopropylethyl amine (9.85 g, 76.2 mmol) was added dropwise to a 0° C. solution of 4-penten-1-ol (7.22 g, 83.9 mmol) and triphosgene (11.3 g, 38.1 mmol) in 160 mL dioxane. The resulting white suspension was stirred for 5 minutes at 0° C., then allowed to warm to 25° C. over 1 hour. The suspension was cooled to 0° C. with an ice bath and 1 N NaOH (76.2 mL) and L-t-butylglycine (10.0 g, 76.2 mmol) were added. The reaction mixture was warmed to 25° C. and stirred for 18 hours. The dioxane was removed in vacuo and the reaction mixture was basified to pH 12 with 1 N NaOH. The aqueous layer was extracted with DCM (3×150 mL), then acidified to pH˜1 with 6 N HCl. The aqueous layer was extracted with DCM (3×150 mL). The combined organic layers were dried over MgSO4 and concentrated to give the compound as a tan oil (13.7 g, 73.9% yield). LRMS (ESI) m/z 244 [(M+H)+; calcd for C12H22NO4 244].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08377873B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-b6397d4c317d4728ba5e258f4cfa1ffb
Quellennotizuspto-grants-2013_02