Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 373549Erstellt: 23. Oktober 2026

Iodine → 2,3,4,5-Tetrahydro-alpha-methyl-1-benzoxepine-8-methanol

https://huagongshe.com/de/reaction/373549

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTetrahydrofuranHCID 8028—
Edukt8-Bromo-2,3,4,5-tetrahydrobenzo[b]oxepineHCID 19935534—
Katalysator1,2-DibromoethaneHCID 7839—
Produkt2,3,4,5-Tetrahydro-alpha-methyl-1-benzoxepine-8-methanolHCID 19935427—

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

7.3 g of 8-bromo-2,3,4,5-tetrahydro-1-benzoxepine in 30 ml of absolute tetrahydrofuran were added under argon to 930 mg shavings and a granule of iodine. The reaction was intitiated by the addition of a few drops of 1,2-dibromoethane and has finished after 2 hours. Thereafter, the reaction mixture was cooled to -10° C. and excess acetaldehyde was distilled into the reaction vessel. After 10 minutes, the mixture was hydrolyzed with saturated sodium bicarbonate (NaHCO3) solution, extracted with ether, washed with water, dried and evaporated to dryness. Chromatography on silica gel (petroleum ether/ethyl acetate 3:1) yielded 4.93 g of 2,3,4,5-tetrahydro-α-methyl-1-benzoxepine-8-methanol as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05164387
Quelldatensatzuspto-grants-1992_11
ORD IDord-c8c67de915d2404f9289478b5992c195
Quellennotizuspto-grants-1992_11