HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 508626Erstellt: 26. Oktober 2026
Bromoacetonitrile → N-((1-(cyanomethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide
https://huagongshe.com/reaction/508626
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromoacetonitrile | HCID 11534 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-(piperidin-4-ylmethyl)-3,5-bis(trifluoromethyl)benzamide | HCID 57993323 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | N-((1-(cyanomethyl)piperidin-4-yl)methyl)-3,5-bis(trifluoromethyl)benzamide | HCID 86636686 | — |
Reaktionsschritte
N-(piperidin-4-ylmethyl)-3,5-bis(trifluoromethyl)benzamide (3.54 g, 10.0 mmol) was dissolved in CH3CN (100 mL). DIPEA (1.94 g, 15.0 mmol) and bromoacetonitrile (1.32 g, 11.0 mmol) were added. The reaction mixture was heated at 50° C. overnight. The solvent was removed in vacuo. Saturated NaHCO3 (40 mL) was added and the mixture was extracted with CH2Cl2 (4×30 mL). The combined organic solution was dried over anhydrous Na2SO4 and passed through a silica gel plug. The desired compound was eluted off with EtOAc. The product was further purified by crystallization from EtOAc/petroleum ether as a white solid (3.62 g, 92%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09096522B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-e6b1bc3ae9eb40999b2fabeb7d6cc954 |
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| Quellennotiz | uspto-grants-2015_08 |
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