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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 732815Erstellt: 24. Oktober 2026

6-Methoxy-1-benzothiophene → Benzo(b)thiophene-6-ol

https://huagongshe.com/de/reaction/732815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Methoxy-1-benzothiopheneHCID 13634237—
EduktHCID 45051917HCID 45051917—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzo(b)thiophene-6-olHCID 8800436,5%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

Dissolve 6-methoxy-benzo[b]thiophene (J. Med. Chem. 32:2548, 1989; 26.1 g, 146 mmol) in DMF (500 mL). Add ethanethiol sodium salt (37 g, 440 mmol) and heat to 150° C. with stirring overnight. Add additional ethanethiol sodium salt (12.8 g, 152 mmol) and continue to heat at 150° C. overnight. Concentrate in vacuo to ¼ volume. Partition reaction mixture between ethyl acetate (500 mL) and water (500 mL), separate layers, wash organic layer with water (2×500 mL), brine (500 mL), and dry with magnesium sulfate. Filter and concentrate in vacuo to give 8 g of benzo[b]thiophen-6-ol. Back extract aqueous layers with ethyl acetate (3×1000 mL) wash organics with brine, and dry with magnesium sulfate. Concentrate in vacuo to obtain an additional 15 grams of benzo[b]thiophen-6-ol. Distill off remaining DMF to yield 22.7 g (100%) of benzo[b]thiophen-6-ol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07585977B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-6527434e7a064093bc3627e0d06acd05
Quellennotizuspto-grants-2009_09