HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444661Erstellt: 26. Oktober 2026
Hydrochloric Acid → 3,7-Dibromodibenzo(b,d)thiophene
https://huagongshe.com/reaction/444661
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 3,7-Dibromo-dibenzothiophene 5,5-dioxide | HCID 4071898 | — |
| Edukt | Aluminium lithium hydride | HCID 21226445 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | 3,7-Dibromodibenzo(b,d)thiophene | HCID 803759 | 48,1% |
Reaktionsschritte
In a 500-ml flask, lithium aluminum hydride (4.1 g) is slowly introduced in small amounts over 50 minutes into a mixture of 3,7-dibromodibenzothiophene dioxide (20 g) and anhydrous ether (200 ml) in an ice bath, and the resulting mixture is refluxed and stirred for 2 hours. Water (200 ml) is added thereto to deactivate lithium aluminum hydride. Chloroform (200 ml) and concentrated hydrochloric acid (40 ml) are added thereto, the mixture is thoroughly stirred, and the organic layer is separated. The aqueous layer is further extracted with chloroform (200 ml×2), the chloroform extract is combined with the organic layer, and the combined organic layer is washed with water (200 ml) and saturated brine (200 ml), and dried over calcium chloride. The solvent is distilled off, and colorless crystals thus obtained are recrystallized from ethyl acetate+ethanol (16:3). Thus, 8.8 g of 3,7-dibromodibenzothiophene is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08475984B1 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-e8993a482e264607916821b1a435b3a0 |
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| Quellennotiz | uspto-grants-2013_07 |
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