HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242624Erstellt: 25. Oktober 2026
4-Chloro-2-nitrobenzaldehyde → HCID 66758130, Verbindung
https://huagongshe.com/reaction/242624
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Chloro-2-nitrobenzaldehyde | HCID 79674 | — |
| Edukt | 1-Boc-3-aminopyrrolidine | HCID 2756370 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 66758130 | HCID 66758130 | — |
Reaktionsschritte
To a solution of 3-Amino-pyrrolidine-1-carboxylic acid tert-butyl ester (2 g, 10.7 mmol) in methanol (20 mL) was added 4-Chloro-2-nitro-benzaldehyde (1.98 g, 10.7 mmol). The resultant solution was heated at 60° C. overnight. The reaction mixture was cooled to 0° C. and to it was added NaBH4 (629 mg, 10 mmol). After 1 h, the reaction solution was quenched with saturated NaHCO3 solution and extracted with ethyl acetate. The organic extract was dried over MgSO4, filtered and concentrated to provide the crude product as an oil. The crude product was used in the subsequent reaction without further purification. LCMS (retention time=1.28, ES+; 356)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653096B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-816b0c49c9614adb8740b35af458b82f |
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| Quellennotiz | uspto-grants-2014_02 |
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