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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7849Erstellt: 23. Oktober 2026

Boron tribromide → 9a-BUTYL-7-HYDROXY-8-METHYL-1,2,9,9a-TETRAHYDRO-3H-FLUOREN-3-ONE

https://huagongshe.com/de/reaction/7849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron tribromideHCID 25134—
Edukt9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 21990884—
LösungsmittelDichloromethaneHCID 6344—
Produkt9a-BUTYL-7-HYDROXY-8-METHYL-1,2,9,9a-TETRAHYDRO-3H-FLUOREN-3-ONEHCID 996527299,1%

Reaktionsschritte

A solution of 9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (28.4 mg, 0.1 mmol) in anhydrous CH2Cl2 (1.7 mL) was stirred under a nitrogen atmosphere and cooled in a dry ice-acetone bath while 1M BBr3 in CH2Cl2 (0.30 mL, 0.3 mmol) was added dropwise by syringe. The cooling bath was removed and the reaction mixture was stirred at room temperature for 4 hours. The mixture was diluted with EtOAc (8 mL), water (3 mL) and 1N HCL (1 mL) and shaken vigorously. The EtOAc layer was separated, washed with water (3 mL), 1M pH 3 phosphate (3 mL) and brine (3 mL), dried over MgSO4, filtered and evaporated under vacuum to give an ochre solid (26.8 mg). The crude product was suspended in CDCl3 (1 mL) and filtered. The solid portion was dried under vacuum to afford 9a-butyl-7-hydroxy-8-methyl-1,2,9,9a-3H-tetrahydro-fluoren-3-one as an olive colored powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087599B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-a3003665ff944b9aba117505583cfbac
Quellennotizuspto-grants-2006_08