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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Iodine | HCID 807 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 8-Bromo-2,3,4,5-tetrahydrobenzo[b]oxepine | HCID 19935534 | — |
| Katalysator | 1,2-Dibromoethane | HCID 7839 | — |
| Produkt | 2,3,4,5-Tetrahydro-alpha-methyl-1-benzoxepine-8-methanol | HCID 19935427 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05300522 |
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| Quelldatensatz | uspto-grants-1994_04 |
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| ORD ID | ord-9174c5fde683479b9293a27fac732da6 |
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| Quellennotiz | uspto-grants-1994_04 |
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