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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 485041Erstellt: 24. Oktober 2026

Propargyl bromide → 2-(N-methyl-N-propynylamino)benzothiazole

https://huagongshe.com/de/reaction/485041

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropargyl bromideHCID 7842—
EduktHexaneHCID 8058—
EduktN-Methylbenzothiazol-2-amineHCID 28160—
EduktButyllithiumHCID 178418339—
LösungsmittelChloroformHCID 6212—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(N-methyl-N-propynylamino)benzothiazoleHCID 2027133384%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

2-Methylaminobenzothiazole (c) (14.0 g) was dissolved in anhydrous tetrahydrofuran (250 ml) and a hexane solution (73 ml) of butyl lithium (6.53 g) was added thereto at -78° C. with stirring. The mixture was stirred for 1.5 hours under cooling and 2-propynyl bromide (8.4 ml) was dropwise added thereto. The resultant mixture was allowed to stand at room temperature overnight and then evaporated to remove the solvent. After addition of water, the residue was extracted with ether. The extract was washed with water, dried and evaporated to remove the solvent. The resultant residue was applied to column chromatography on silica gel (280 g) to give 2-(N-methyl-N-propynylamino)benzothiazole (d) (14.5 g, yield 84%) from chloroform eluate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04535088
Quelldatensatzuspto-grants-1985_08
ORD IDord-655eb8d90eae40d1a7ee035d7ffa7030
Quellennotizuspto-grants-1985_08