HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1010545Erstellt: 25. Oktober 2026
Sulfuric acid magnesium salt (1:1) → (tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl](oxolan-3-ylmethyl)amino}ethyl)carboxamide
https://huagongshe.com/reaction/1010545
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Edukt | 3-Furancarboxaldehyde, tetrahydro- | HCID 157568 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | Tert-butyl N-(2-{[(4-methoxyphenyl)methyl]amino}ethyl)carbamate | HCID 112688707 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | (tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl](oxolan-3-ylmethyl)amino}ethyl)carboxamide | HCID 131728997 | 80,9% |
Reaktionsschritte
This compound was made in a manner analogous to that set forth in Step D of Example 5, using 0.2 gram (0.0020 mole) of (oxolan-3-yl)formaldehyde, 0.56 gram (0.0020 mole) of (tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl]amino}-ethyl)carboxamide (prepared in Step A of Example 9), 0.64 gram (0.0030 mole) of sodium triacetoxyborohydride and 2.5 grams (0.021 mole) of magnesium sulfate in 50 mL of 1,2-dichloroethane. The reaction product was purified with column chromatography on silica gel. Elution was accomplished using a mixture of 1% methanol in methylene chloride as an eluant. Appropriate fractions were combined and concentrated under reduced pressure, yielding 0.59 gram of the subject compound. The NMR spectrum was consistent with the proposed structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07977332B2 |
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| Quelldatensatz | uspto-grants-2011_07 |
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| ORD ID | ord-ab9d4328df8b41dcbeb9a02578764ec8 |
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| Quellennotiz | uspto-grants-2011_07 |
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