Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 6-Methoxy-1-benzothiophene | HCID 13634237 | — |
| Edukt | HCID 45051917 | HCID 45051917 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Benzo(b)thiophene-6-ol | HCID 88004 | 36,5% |
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 heats to 150° C. with stirring overnight. Add additional ethanethiol sodium salt (112.8 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 mf), 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07399867B2 |
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| Quelldatensatz | uspto-grants-2008_07 |
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| ORD ID | ord-1a9dd29be33747dfb270fc730af6dd47 |
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| Quellennotiz | uspto-grants-2008_07 |
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