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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132936Erstellt: 25. Oktober 2026

Hydrogen Peroxide → (S)-2-((R)-3-isopropyl-2-oxopyrrolidin-1-yl)-4-phenylbutanoic acid

https://huagongshe.com/reaction/132936

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktLithium HydroxideHCID 3939—
Edukt(R)-2-isopropylpent-4-enoic acidHCID 6915842—
Edukt(2R,4R)-tert-butyl 4-(allyloxy)-2-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 67315914—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(S)-2-((R)-3-isopropyl-2-oxopyrrolidin-1-yl)-4-phenylbutanoic acidHCID 69193934—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Step D (3): (R)-2-isopropylpent-4-enoic acid. To a solution of the compound of step D (2) (1.08 g, 3.59 mmol) in THF (14.4 mL) was added water (3.59 mL), and the mixture cooled to 0° C. A solution of LiOH (172.5 mg, 7.20 mmol) and 30% H2O2 (3.26 mL) in water (11.2 mL) was added, and the combined mixture stirred for 10 minutes at 0° C. The ice bath was removed, and the reaction was allowed to continue for 1 h at rt. A solution of sodium sulfite (3.63 g) was added, and the reaction stirred for 10 min. Saturated sodium carbonate solution was added, and the reaction was extracted with methylene chloride. The aqueous layer was acidified to pH 1 with 6 N HCl, and extracted 3 times with diethyl ether. The combined ether layers were washed with brine, and dried over MgSO4. The extract was filtered, and concentrated in vacuo to afford the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07388007B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-283a997f1521485da8e04a718d140aab
Quellennotizuspto-grants-2008_06