HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2309725Erstellt: 25. Oktober 2026
Potassium Carbonate → N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide, (S)-
https://huagongshe.com/reaction/2309725
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Edukt | (2S)-2-Aminobutanamide hydrochloride | HCID 11961924 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | N-(1-Amino-1-oxobutan-2-yl)-4-chlorobutanamide, (S)- | HCID 29938341 | 78,7% |
Reaktionsschritte
345.6 g (2.5 moles) of ground potassium carbonate are mixed with 138.5 g (1 mole) of (S)-2-amino-butanamide hydrochloride in 2.5 liters of acetonitrile. The reaction mixture is cooled to 0° C. and a solution of 129.2 g (1.2 mole) of 4-chlorobutyryl chloride in 500 ml of acetonitrile is introduced dropwise. After the addition, the reaction mixture is allowed to return to ambient temperature; the insoluble matter is filtered off and the filtrate evaporated under reduced pressure. The crude residue obtained is stirred in 1.2 liter of anhydrous ether for 30 minutes at a temperature between 5° and 10° C. The precipitate is filtered off, washed twice with 225 ml of ether and dried in vacuo to obtain 162.7 g of (S)-N-[1-(aminocarbonyl)propyl]-4-chlorobutanamide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04696943 |
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| Quelldatensatz | uspto-grants-1987_09 |
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| ORD ID | ord-e663bdd7493e4838b3ea41f125430c86 |
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| Quellennotiz | uspto-grants-1987_09 |
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