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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 58966Erstellt: 24. Oktober 2026

Isophthalaldehyde → Di-tert-butyl (((((1,3-phenylenebis(methylene))bis(azanediyl))bis(propane-3,1-diyl))bis(azanediyl))bis(propane-3,1-diyl))dicarbamate

https://huagongshe.com/de/reaction/58966

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsophthalaldehydeHCID 34777—
Edukt1,1-Dimethylethyl N-(3-((3-aminopropyl)amino)propyl)carbamateHCID 2786632—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
ProduktDi-tert-butyl (((((1,3-phenylenebis(methylene))bis(azanediyl))bis(propane-3,1-diyl))bis(azanediyl))bis(propane-3,1-diyl))dicarbamateHCID 117633421—

Reaktionsschritte

Isophthalaldehyde (1.07 g, 7.99 mmol) and MeOH (50 mL) were added to a round-bottom flask. To the solution was added tert-butyl (3-((3-aminopropyl)amino)propyl)carbamate (3.69 g, 16.0 mmol) and the reaction mixture was stirred for 24 h. Sodium borohydride (1.21 g, 32.0 mmol) was added portionwise and stirred for 1 h. The reaction mixture was concentrated under reduced pressure, and aq. NaOH (10%, 150 mL) and EtOAc (150 mL) were added. The layers were separated, and the aqueous layer was extracted with EtOAc (150 mL). The organic layers were combined, dried over Na2SO4, filtered, and concentrated under reduced pressure to afford the desired product as a clear oil. The intermediate was carried forward without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09439433B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-c68bf2c627ce430aa507bc115a2b1ecb
Quellennotizuspto-grants-2016_09