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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1418791Erstellt: 27. Oktober 2026

Acetic Acid → N-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanol

https://huagongshe.com/reaction/1418791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktMethanolHCID 887—
EduktSodium borohydrideHCID 4311764—
EduktN-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl esterHCID 22940772—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
ProduktN-Benzyloxycarbonyl-2-amino-2-[4-propoxybenzyl]-ethanolHCID 67688130—

Reaktionsschritte

4.15 g (11.2 mmol) of N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester is dissolved in 20 ml of tert-butyl methyl ether and mixed with 0.17 g (4.5 mmol) of sodium borohydride. At 0° C., 6 ml of methanol is added and it is stirred for three hours under argon at a temperature below 5° C. Then, 0.8 ml of acetic acid, dissolved in 3 ml of tetrahydrofuran, is added, mixed with 3 ml of water and stirred for ten minutes at room temperature. The organic phase is separated, washed with water and dried on sodium sulfate. The drying agent is suctioned off, the filtrate is concentrated by evaporation and the residue is chromatographed for purification on silica gel (eluent: ethyl acetate/hexane).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05885548
Quelldatensatzuspto-grants-1999_03
ORD IDord-618e053887574cc6b247533a9ccc844b
Quellennotizuspto-grants-1999_03