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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenyltrimethylammonium bromide dibromideHCID 17977687—
Edukt1-(Benzo[b]thiophen-7-yl)propan-1-oneHCID 22473897—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(Benzo[b]thiophen-7-yl)-2-bromopropan-1-oneHCID 22474143112,5%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06900216B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-8f8daf008bb5407a9b9d5c9062fb3418
Quellennotizuspto-grants-2005_05