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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1463394Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1463394

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
PatentnummerUS05300522
Quelldatensatzuspto-grants-1994_04
ORD IDord-9174c5fde683479b9293a27fac732da6
Quellennotizuspto-grants-1994_04