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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246882Erstellt: 25. Oktober 2026

Butanedione → 3-Hydroxy-3-phenylbutan-2-one

https://huagongshe.com/reaction/246882

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButanedioneHCID 650—
EduktTolueneHCID 1140—
EduktTetrahydrofuranHCID 8028—
EduktHCID 178418255HCID 178418255—
LösungsmittelTetrahydrofuran tolueneHCID 22635083—
Produkt3-Hydroxy-3-phenylbutan-2-oneHCID 23322068%

Reaktionsschritte

The process can also be run in mixtures of tetrahydrofuran and toluene, thereby making the process more economical. When 1.1 equivalent of phenylmagnesium bromide (1.9M in 50% THF/PhMe) was added to 2,3-butanedione in 50% THF/PhMe, crude product was isolated in 82.4% yield (Run 10, Table IV) after work-up. Short path vacuum distillation gave 3-hydroxy-3-phenylbutan-2-one in 68% yield. Alternatively, preparation of phenylmagnesium bromide in 38% THF/PhMe, followed by reaction with 2,3-butanedione in 38% THF/PhMe afforded 3-hydroxy-3-phenylbutan-2-one in 66.4% yield (Run 11, Table IV) after work-up and distillation. Similarly phenylmagnessium bromide in 25% THR/PheMe reacted with 2,3-butanedione in 25% THF/PheMe yielded 3-hydroxy-3-phenylbutan-2-one in 56.9% yield after work-up and distillation.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04704475
Quelldatensatzuspto-grants-1987_11
ORD IDord-cede89cb38c04486bb9c278853a2f81c
Quellennotizuspto-grants-1987_11