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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12993Erstellt: 24. Oktober 2026

Diisopropylethylamine → E-3-[4'-hydroxybiphenyl-3-yl]-N-hydroxyacrylamide

https://huagongshe.com/de/reaction/12993

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktHydroxyamine hydrochlorideHCID 443297—
EduktMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
EduktE-3-(4'-hydroxybiphenyl-3-yl)-acrylic acidHCID 22475282—
LösungsmittelDimethylformamideHCID 6228—
ProduktE-3-[4'-hydroxybiphenyl-3-yl]-N-hydroxyacrylamideHCID 4263237032,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

70 mg (0.29 mmol) of E-3-(4′-hydroxybiphenyl-3-yl)-acrylic acid were dissolved under nitrogen in 3 ml of DMF, then 109 mg (0.29 mmol) of HBTU and 100 μL (0.57 mmol) of DIPEA were added at 0° C. After 5 min hydroxylamine hydrochloride (20 mg, 0.29 mmol) was added and the mixture was stirred at 0° C. for 10 min., then at room temperature for 4 h. DMF was removed under reduced pressure and the residue was washed with water to obtain, after filtration, 73 mg of a crude product. Purification by flash chromatography on KH2PO4 buffered silicagel using as eluent CH2Cl2/MeOH 95:5 afforded 24 mg of the title compound as a white solid. M.p. 127-128° C. Rf=0.26 (Merck silica gel 60F254, CH2Cl2:/MeOH 90:10)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728039B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-310f30a16ec54f1182a25511c29bcf0a
Quellennotizuspto-grants-2010_06