HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 467840Erstellt: 25. Oktober 2026
Acetic Acid → 4-Cyclopropylmorpholine-3-carboxamide
https://huagongshe.com/reaction/467840
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Trimethylsilane | HCID 70435 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | Morpholine-3-carboxylic acid amide hydrochloride | HCID 67166308 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-Cyclopropylmorpholine-3-carboxamide | HCID 67153953 | 47,3% |
Reaktionsschritte
2.9 g of molecular sieve 3A, 4.3 g (72 mmol) of acetic acid, 7.6 g (43.2 mmol) of 2(1-ethoxy-cyclopropyl)oxy]trimethylsilane and 4.4 g (31.7 mmol) of sodium cyanoborohydride are added successively to 1.2 g (7.2 mmol) of morpholine-3-carboxylic acid amide hydrochloride (WO2005026156 Hennequin L. F. A. et al.) in solution in methanol (36 ml). The reaction mixture is heated at 70° C. for 3.5 hours, then cooled to room temperature and filtered. The filtrate is concentrated under reduced pressure, then the residue is taken up in dichloromethane (200 ml) and washed 3 times with an aqueous solution of NaOH (1N) (100 ml). The organic phase is dried over Na2SO4, filtered and then concentrated under reduced pressure. 0.58 g of product is obtained, in the form of a white powder. Yield 47%. Melting point 116° C. MH+: 171 (Tr: 1.03 min, condition 2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08623893B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-a86fd0b35bc34d6f9c669a22b5a5f379 |
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| Quellennotiz | uspto-grants-2014_01 |
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