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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1478885Erstellt: 25. Oktober 2026

Water → 2-(3,4-Bis(2-(tert-butoxycarbonylamino)ethoxy)phenyl)acetic acid

https://huagongshe.com/reaction/1478885

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
Edukttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
EduktMethyl 3,4-DihydroxyphenylacetateHCID 11008556—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium HydroxideHCID 14798—
Produkt2-(3,4-Bis(2-(tert-butoxycarbonylamino)ethoxy)phenyl)acetic acidHCID 86725281—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To methyl 2-(3,4-dihydroxyphenyl)acetate (1.0 g) in DMF (10 mL) was added tert-butyl 2-bromoethylcarbamate (2.7 g) and K2CO3 (1.7 g). The resulting reaction mixture was stirred at 60° C. overnight. Water was added and the aqueous phase extracted with EtOAc. The organic phase was then dried and concentrated. The residue was purified by flash chromatography. The product was obtained as a mixture of mono- and bis-alkylation. The mixture was then dissolved in MeOH and THF (10 mL, 1:1) and IN NaOH was added. The resulting reaction mixture was stirred at room temperature overnight. IN HCl was added to acidify the solution. The aqueous phase was extracted with EtOAc (3×). The organic phases were combined, dried and concentrated. The title product was obtained by reverse phase chromatography purification (0.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09403850B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-c12e81b672324999a5c61d59ee958931
Quellennotizuspto-grants-2016_08