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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1772306Erstellt: 25. Oktober 2026

Benzoyl chloride → (S)-beta-Benzoyloxy-gamma-butyrolactone

https://huagongshe.com/reaction/1772306

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
Edukt3-Hydroxybutyrolactone, (3S)-HCID 7269389—
LösungsmittelPyridineHCID 1049—
Produkt(S)-beta-Benzoyloxy-gamma-butyrolactoneHCID 1005879989%

Reaktionsschritte

To the solution of (S)-β-Hydroxy-γ-butyrolactone (1.0 g, 9.8 mmol) in 25 mL pyridine was added dropwise BzCl (1.4 mL, 12.2 mmol) at 0° C. The reaction mixture was warmed to room temperature and stirred overnight. The reaction was concentrated and coevaporated with toluene two times in vacuo. The residue was partitioned between H2O (15 mL) and EtOAc (40 mL). The organic layer was washed with water and brine, and concentrated in vacuo. The residue was purified by chromatography on a silica gel column (n-hexane/EtOAc=8:1) to afford 101 (1.78 g, 8.6 mmol) as a white solid, in 89% yield, which was characterized as follows:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09249177B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-41730e38b7e84917a0199cd983cacb83
Quellennotizuspto-grants-2016_02