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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Edukt3-Furancarboxaldehyde, tetrahydro-HCID 157568—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktTert-butyl N-(2-{[(4-methoxyphenyl)methyl]amino}ethyl)carbamateHCID 112688707—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt(tert-butoxy)-N-(2-{[(4-methoxyphenyl)methyl](oxolan-3-ylmethyl)amino}ethyl)carboxamideHCID 13172899780,9%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07977332B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-ab9d4328df8b41dcbeb9a02578764ec8
Quellennotizuspto-grants-2011_07