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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37412Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/37412

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 of Mg shavings and a granule of iodine. The reaction was initiated by the addition of a few drops of 1,2-dibromoethane and had 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
PatentnummerUS05420273
Quelldatensatzuspto-grants-1995_05
ORD IDord-69558ce886804b19993bb5e130032ad6
Quellennotizuspto-grants-1995_05