Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234165Erstellt: 26. Oktober 2026

Phenethyl bromide → 3-(2-phenylethyl)-1,3-benzothiazol-2(3H)-one

https://huagongshe.com/reaction/234165

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethyl bromideHCID 7666—
EduktBenzothiazoloneHCID 13625—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
EduktHCID 178418361HCID 178418361—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(2-phenylethyl)-1,3-benzothiazol-2(3H)-oneHCID 109314680%

Reaktionsschritte

(1aB) Benzothiazolin-2-one (5.15 g, 34.1 mmol) was dissolved in dimethylformamide (100 ml) and to the solution was added 60% sodium hydride (1.36 g, 34.1 mmol) which was stirred at room temperature until generation of hydrogen gas stopped. Then β-phenylethylbromide (4.89 ml, 35.8 mmol) was added to the solution which was stirred at room temperature for 17 hours. To the reaction solution was added a saturated aqueous solution of ammonium chloride, followed by extraction with ethyl acetate. The organic layer was washed in turn with a saturated sodium bicarbonate solution and saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The crude product thus obtained was purified by subjecting it to silica gel column chromatography to give 6.49 g of 3-phenethylbenzothiazoline-2-one as a white amorphous powder form n-hexane/ethyl (4:1)-eluted fraction (yield: 80%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594144
Quelldatensatzuspto-grants-1997_01
ORD IDord-456553774f75411b9d86aa476cb84047
Quellennotizuspto-grants-1997_01