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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27348Erstellt: 23. Oktober 2026

Gamma-Aminobutyric Acid → 4-(((Benzyloxy)carbonyl)amino)butanoic acid

https://huagongshe.com/de/reaction/27348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGamma-Aminobutyric AcidHCID 119—
EduktWaterHCID 962—
EduktBenzyl succinimido carbonateHCID 83172—
EduktSodium BicarbonateHCID 516892—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(((Benzyloxy)carbonyl)amino)butanoic acidHCID 21184—

Reaktionsschritte

To a solution of 100 ml. of water and 120 ml. of tetrahydrofuran is added sequentially 12.4 g. of γ-aminobutyric acid, 10.4 g. of sodium bicarbonate, and 30 g. of N-benzyloxycarbonyloxysuccinimide. The reaction mixture is stirred for approximately 3.5 hours at room temperature and then the tetrahydrofuran is evaporated in vacuo. The residue is diluted with 200 ml. of water and extracted with (2×300 ml.) anhydrous ether. The aqueous layer is then acidified to pH 1-2 with 1 N hydrochloric acid and extracted with (3×400 ml.) methylene chloride. The methylene chloride extracts are collected and combined and then washed with (3×200 ml.) brine solution, dried with anhydrous magnesium sulfate and the solvent evaporated in vacuo at room temperature. The residue provides N-carbobenzoxy-γ-aminobutyric acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04221706
Quelldatensatzuspto-grants-1980_09
ORD IDord-ea43e1971c3f40c79b2c67c5c1bb1432
Quellennotizuspto-grants-1980_09