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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 369564Erstellt: 23. Oktober 2026

Sulfuric Acid → 6-Methoxy-1,3-benzothiazole-2-carbaldehyde

https://huagongshe.com/de/reaction/369564

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktDiethyl EtherHCID 3283—
Edukt2-Cyano-6-methoxy benzothiazoleHCID 342109—
EduktAluminium lithium hydrideHCID 21226445—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-Methoxy-1,3-benzothiazole-2-carbaldehydeHCID 1459898130,5%

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

2-Cyano-6-methoxybenzothiazole (10.0 g, 52.6 mmol) was suspended in a mixture of anhydrous ether (400 ml) and 2-propanol (36 ml). The suspension was cooled to about -30° C. by a dry-ice bath. Lithium aluminum hydride (7.0 g, 184.5 mmol) was added slowly while keeping the reaction temperature below -30° C. under argon atmosphere. The reaction mixture was stirred for 1 hr after the addition of lithium aluminum hydride and then poured slowly into a mixture of 2 N sulfuric acid (900 ml) and ethyl acetate (500 ml). After stirring for 10 min the organic layer was separated and the aqueous layer was extracted with ethyl acetate (200 ml). The combined organic phase was washed with water (200 ml) and then dried with anhydrous sodium sulfate (50 g) overnight. The dried solution was concentrated and then flash chromatographed on silica gel to give 3.1 g (30.5%) of a yellowish solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06140051
Quelldatensatzuspto-grants-2000_10
ORD IDord-b79409986bce4557842dedb76cbd3450
Quellennotizuspto-grants-2000_10