HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 886754Erstellt: 25. Oktober 2026
Tert-Butylamine → 5-bromo-N-tert-butylthiophene-2-carboxamide
https://huagongshe.com/reaction/886754
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Tert-Butylamine | HCID 6385 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 5-Bromothiophene-2-carboxylic acid | HCID 349115 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-bromo-N-tert-butylthiophene-2-carboxamide | HCID 845090 | 83,4% |
Reaktionsschritte
A mixture of 5-bromothiophene-2-carboxylic acid (10.0 g, 48 mmol) and thionyl chloride (3.5 ml, 48 mmol) was boiled under reflux for 3 hrs. Excess of thionyl chloride was removed by distillation under reduced pressure. The residue was taken up in DCM (30 ml) and a solution of tert-butylamine (7.0 g, 96 mmol) in DCM (30 ml) was added with stirring, the temperature of the mixture being kept below 10° C. The resulting solution was stirred at 25° C. for 12 hrs, washed with water (3×20 ml) and dried over MgSO4. The combined washings were basified to pH11 with 5M KOH(aq) and extracted with DCM (3×100 ml) and dried over MgSO4. The combined organic solutions were evaporated under reduced pressure to give the crude product (12.5 g). Recrystallization from (C6H12/CHCl3) gave the pure amide (10.5 g) as a white solid. MS (ES+): 263 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08247409B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-2970e4ab3f584aaab36dc1ceb332d458 |
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| Quellennotiz | uspto-grants-2012_08 |
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