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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 657482Erstellt: 24. Oktober 2026

(S)-beta-Benzoyloxy-gamma-butyrolactone → 3-O-benzoyl-2-deoxy-threose

https://huagongshe.com/de/reaction/657482

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(S)-beta-Benzoyloxy-gamma-butyrolactoneHCID 10058799—
EduktDiisopropylaluminium hydrideHCID 21896610—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-O-benzoyl-2-deoxy-threoseHCID 8666451375%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 101 (0.780 g, 3.8 mmol) in 13 mL dry THF was slowly dropwise added 1.0 M diisopropyl aluminiumhydride (4.7 mL, 4.7 mmol) in toluene at −78° C. The reaction mixture was stirred at −78° C., and as soon as the starting material was completely consumed (TLC, 2 hours), methanol (2 mL) was slowly added in order to quench the reaction. The cooling bath was removed, 15 mL of a saturated aqeous sodium potassium tartrate solution and 25 mL of EtOAc were added and the mixture stirred vigorously for 3 hours. The organic layer was washed with water and brine, and concentrated under vacuo. The residue was purified by chromatography on a silica gel column (n-hexane/EtOAc=8:2) to afford 102 (590 mg, 2.8 mmol) as a colorless oil, in 75% yield, which was characterized as follows:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08076310B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-6318b25e1268499eb24d004cf7576553
Quellennotizuspto-grants-2011_12