HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370983Erstellt: 24. Oktober 2026
Dimethylformamide → 6,7-Dichloro-2-formyl-5-hydroxybenzo[b]thiophene
https://huagongshe.com/de/reaction/370983
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 6,7-Dichloro-1-benzothiophene-5-ol | HCID 13289997 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6,7-Dichloro-2-formyl-5-hydroxybenzo[b]thiophene | HCID 13290037 | — |
Reaktionsschritte
A solution of 8.7 g of 6,7-dichloro-5-hydroxybenzo[b]thiophene in 50 ml of anhydrous tetrahydrofuran is placed in a 250 ml 3-necked flask and cooled to -25°. To the solution under nitrogen, is added dropwise 42 ml of a solution of 2.5M n-butyllithium at a rate such that the temperature did not rise above -10°. After total addition, the mixture is stirred at 0°-5° for 3 hrs. To the mixture is added 14 ml of anhydrous dimethylformamide over a period of 20 mins. The reaction mixture is allowed to warm to room temperature and stirred for 1 hr. Quenching with 400 ml of 2N hydrochloric acid, followed by extraction with ethyl acetate, gives a precipitate. Recrystallization from acetone-hexane affords 6.5 g of 6,7-dichloro-2-formyl-5-hydroxy-benzo[b]thiophene, mp 197°-198°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04528399 |
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| Quelldatensatz | uspto-grants-1985_07 |
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| ORD ID | ord-89a7fe1f5cec422fb7718e66405f20c6 |
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| Quellennotiz | uspto-grants-1985_07 |
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