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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1698479Erstellt: 25. Oktober 2026

Glycidyl benzoate → 2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate

https://huagongshe.com/reaction/1698479

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGlycidyl benzoateHCID 25998—
EduktN-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanineHCID 14217229—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelTolueneHCID 1140—
Produkt2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoateHCID 6020725226%

Reaktionsschritte

A solution of oxiran-2-ylmethyl benzoate (3.0 g, 16.8 mmol), (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoic acid (6.0 g, 20.2 mmol), and tetrabutylammonium bromide (542 mg, 1.7 mmol) in anhydrous toluene was heated to 90° C. for 18 hrs. The reaction mixture was concentrated to dryness under reduced pressure, diluted with ethyl acetate, and washed with water twice followed by the addition of a saturated NaHCO3 solution and brine. The organic layer was dried through MgSO4 and concentrated under reduced pressure. Chromatography (silica gel, 1:1 ethyl acetate/hexane) of the residue afforded 2.05 g (26%) of 2-Hydroxy-3-phenylcarbonyloxypropyl(2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163958B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-416b80eae45d4fa68561b3347da6f513
Quellennotizuspto-grants-2012_04