HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1869645Erstellt: 25. Oktober 2026
Pyridine → (2S)-1-(2-bromoacetyl)pyrrolidine-2-carbonitrile
https://huagongshe.com/reaction/1869645
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Bromoacetyl bromide | HCID 61147 | — |
| Edukt | (2S)-pyrrolidine-2-carbonitrile | HCID 5706552 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (2S)-1-(2-bromoacetyl)pyrrolidine-2-carbonitrile | HCID 11031276 | 82,6% |
Reaktionsschritte
To a cold solution (−10° C.) of bromoacetyl bromide (2.0 g, 10.0 mmol) in CH2Cl2 (30 mL), a solution of (S)-pyrrolidine-2-carbonitrile (480 mg, 5.0 mmol) and pyridine (1.4 g, 210 mmol) together with a catalytic amount of DMAP (50 mg) in CH2Cl2 (10 mL) was added over a 30 minute period. After stirring for about 10 minutes, the reaction temperature was gradually increased to room temperature. Stirring at room temperature was continued overnight. The residue was diluted with CH2Cl2 (60 mL), washed with ice water and cold 10% sodium bicarbonate aqueous solution to give crude product (1.01 g; yield of 93%). Column chromatography purification of the crude product resulted in pure 1-(2-bromo-acetyl)-(S)-pyrrolidine-2-carbonitrile (892 mg; 82.6% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07638638B2 |
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| Quelldatensatz | uspto-grants-2009_12 |
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| ORD ID | ord-215d032144eb482e9e54cb7de404639e |
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| Quellennotiz | uspto-grants-2009_12 |
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