HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2183655Erstellt: 26. Oktober 2026
Phenyltrimethylammonium bromide dibromide → 1-(Benzo[b]thiophen-7-yl)-2-bromopropan-1-one
https://huagongshe.com/reaction/2183655
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Edukt | 1-(Benzo[b]thiophen-7-yl)propan-1-one | HCID 22473897 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(Benzo[b]thiophen-7-yl)-2-bromopropan-1-one | HCID 22474143 | 112,5% |
Reaktionsschritte
Phenyltrimethylammonium tribromide (1.52 g) was added in portions under nitrogen at 0° C. over 30 minutes to a stirred solution of 1-(benzo[b]thiophen-7-yl)propan-1-one (0.77 g) in tetrahydrofuran (110 ml), then the mixture was stirred at ambient temperature for 18 hours. Further phenyltrimethylammonium tribromide (0.76 g) was added and the mixture was heated under reflux for 4 hours. Further phenyltrimethylammonium tribromide (0.76 g) was added, then the mixture was heated under reflux for 90 minutes, cooled to ambient temperature and filtered. The solvent was removed in vacuo and the residue was purified by flash chromatography over silica using a 7:3 mixture of petroleum ether (b.p. 60-80° C.) and dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 1-(benzo[b]thiophen-7-yl)-2-bromopropan-1-one (0.71 g) as an oil which was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06900216B2 |
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| Quelldatensatz | uspto-grants-2005_05 |
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| ORD ID | ord-8f8daf008bb5407a9b9d5c9062fb3418 |
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| Quellennotiz | uspto-grants-2005_05 |
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