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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444976Erstellt: 25. Oktober 2026

4-Formylbenzoic acid → 4-[(2-tert-Butoxycarbonylethylamino)methyl]benzoic acid

https://huagongshe.com/reaction/444976

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Formylbenzoic acidHCID 12088—
EduktDiisopropylethylamineHCID 81531—
EduktSodium cyanoborohydrideHCID 5003444—
EduktTert-butyl 3-aminopropanoate hydrochlorideHCID 16218890—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt4-[(2-tert-Butoxycarbonylethylamino)methyl]benzoic acidHCID 59687909—

Reaktionsschritte

Tert-butyl 3-aminopropanoate hydrochloride (5 g, 27.7 mmol) was dissolved in methanol (150 mL). Diisopropylethylamin (4.73 mL, 27.7 mmol) was added followed by 4-carboxybenzaldehyd. The mixture is heated to reflux for 1 hour. After cooling to room temperature sodium cyanoborohydride (1.77 g, 22.1 mmol) was added under nitrogen and stirred for 1 hour at room temperature. Acetic acid (15 mL) was added and the mixture was stirred for an additional 1 hour. The mixture was poured into water (300 mL) and stirred at room temperature over night. The water solution was washed with ethyl acetate (3×250 mL). The organic phase dried (Na2SO4) and solvent removed in vacuo to yield the crude product as an oil which solidifies by standing. The crude product was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476228B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-529bb2850dd94b4484bee76555c5f515
Quellennotizuspto-grants-2013_07