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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1112233Erstellt: 27. Oktober 2026

Tetrahydrofuran → (S)-N-Carbobenzyloxy-3-(3,4-diformyloxyphenyl)-2-methylalanine

https://huagongshe.com/reaction/1112233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktAcetic-formic anhydrideHCID 75269—
Edukt(2S)-2-{[(benzyloxy)carbonyl]amino}-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acidHCID 18595367—
Produkt(S)-N-Carbobenzyloxy-3-(3,4-diformyloxyphenyl)-2-methylalanineHCID 54440584100%

Reaktionsschritte

A solution of (S)-N-carbobenzyloxy-3-(3,4-dihydroxyphenyl)-2-methylalanine (0.35 g, 1 mmol) and acetic formic anhydride (0.36 g, 4 mmol) in anhydrous tetrahydrofuran (5 ml) is stirred 24 hours at 20°-25° under dry N2. The solvent is evaporated in vacuo and the residue is dried further at 0.1mm/25° for 2 hours. The product (A) (0.4 g, 100%) is obtained as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04120971
Quelldatensatzuspto-grants-1978_10
ORD IDord-7760bc517207404692cc71f2a5f24c83
Quellennotizuspto-grants-1978_10