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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 236467Erstellt: 25. Oktober 2026

L-Alanine → Boc-Gly-Ala-OH

https://huagongshe.com/reaction/236467

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-AlanineHCID 5950—
EduktTriethylamineHCID 8471—
EduktN-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
EduktN-HydroxysuccinimideHCID 80170—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
ProduktBoc-Gly-Ala-OHHCID 1112859041,5%

Reaktionsschritte

Boc-Gly-Ala-OH was prepared by an N-hydroxysuccinimide coupling procedure. Boc-Gly-OSu (7.67 g, 28.2 mmol) was dissolved in 10 mL of dimethylsulfoxide and the resulting solution was added to a solution consisting of H-Ala-OH (3.76 g, 42.3 mmol) and triethylamine (5.89 mL, 42.3 mmol) in 20 mL of water. After stirring overnight, a precipitate was removed by filtration. The remaining solution was diluted with water and then acidified with hydrochloric acid. An aqueous phase separated from which product was extracted by addition of ethyl acetate. The ethyl acetate extract was washed with 0.2N hydrochloric acid and then saturated sodium chloride prepared in 0.2N hydrochloric acid. The washed ethyl acetate solution was then dried over sodium sulfate and filtered. Solvent was then evaporated, leaving a foamy product, which was crystallized from ethyl acetate:hexane to yield 2.88 g of Boc-Gly-Ala-OH (m.p. 128°-130°).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04644055
Quelldatensatzuspto-grants-1987_02
ORD IDord-5f4e8b8470144a09bcc9d74752d34e24
Quellennotizuspto-grants-1987_02