HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 538863Erstellt: 25. Oktober 2026
Bromine → N-[4-(2-bromobutanoyl)phenyl]acetamide
https://huagongshe.com/reaction/538863
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromine | HCID 24408 | — |
| Edukt | N-(4-Butyrylphenyl)acetamide | HCID 4304236 | — |
| Edukt | Aluminum(III) Chloride | HCID 6451240 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-[4-(2-bromobutanoyl)phenyl]acetamide | HCID 63386157 | — |
Reaktionsschritte
Step-2: A solution of N-(4-butyryl-phenyl)acetamide (3.47 g, 16.9 mmol) in 100 mL of anhydrous DCM was cooled to 0° C. under N, and treated with AlCl3 (180 mg, 1.35 mmol). Approximately 10 mL of Br2 was added and the mixture was stirred for 10 min. The reactor was removed from the cooling bath and the remaining Br2 was added dropwise via syringe over 0.5 min. After 3 hr, the dark orange color of Br2 had faded and by 3¼ hr a precipitate had formed. The reaction was quenched with saturated NaHCO3. The phases were separated and the aqueous phase extracted three times with DCM. The combined extracts were dried over Na2SO4, filtered through a Celite® pad and concentrated in vacuo to give N-(4-(2-bromobutanoyl)phenyl)acetamide which was used without purification. MS ESI: m/z 284.10 [M+].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08865752B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-77dad88af4bb4023a54fc9d7763877b5 |
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| Quellennotiz | uspto-grants-2014_10 |
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