HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 604208Erstellt: 24. Oktober 2026
Methyl iodide → Methyl 6-(benzyloxycarbonyl-methyl-amino)-hexanoate
https://huagongshe.com/de/reaction/604208
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Methyl 6-(benzyloxycarbonylamino)hexanoate | HCID 43404641 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | Methyl 6-(benzyloxycarbonyl-methyl-amino)-hexanoate | HCID 66603267 | — |
Reaktionsschritte
Methyl 6-benzyloxycarbonylamino-hexanoate (4.15 g) is dissolved in N,N-dimethylformamide (2.5 mL) and thereto is added sodium hydride (63%) (552 mg) under ice-cooling and the mixture is stirred at the same temperature for 1 hour and thereto is added methyl iodide (1.72 ml), and the mixture is stirred at the same temperature for an additional 2 hours. To the reaction mixture is added a saturated brine, and the mixture is extracted with ethyl acetate, and the organic layer is washed with a saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give methyl 6-(benzyloxycarbonyl-methyl-amino)-hexanoate (2.25 g). MS (m/z): 294 [M+H]+
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07906517B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-189708985f1b49d6a34171a5bdda60c2 |
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| Quellennotiz | uspto-grants-2011_03 |
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