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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 587233Erstellt: 26. Oktober 2026

Ethyl bromoacetate → ethyl 2-(1-oxo-6-vinylphthalazin-2(1H)-yl)acetate

https://huagongshe.com/reaction/587233

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromoacetateHCID 7748—
EduktCesium carbonateHCID 10796—
Edukt6-vinylphthalazine-1(2H)-oneHCID 86675174—
Edukt1-oxo-6-vinylphthalazine-2(1H)-yl acetateHCID 131734412—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl 2-(1-oxo-6-vinylphthalazin-2(1H)-yl)acetateHCID 8667517345%

Reaktionsschritte

Ethyl-2-(1-oxo-6-vinylphthalazine-2(1H)-yl acetate (BI24): To a stirred solution of 6-vinylphthalazine-1(2H)-one (0.5 g, 2.90 mmol) in DMF (5.0 mL) was added Cs2CO3 (0.94 g, 2.90 mmol) and the reaction was stirred for 10 min Ethyl bromoacetate (0.48 g, 2.90 mmol) was added to the reaction mixture at ambient temperature and the reaction was stirred for 8 h at ambient temperature. The reaction mixture was diluted and extracted with EtOAc, and the EtOAc layer was washed with water and brine solution (2×). The separated EtOAc layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford crude product. The crude compound was purified by column chromatography (SiO2, 100-200 mesh; 25% EtOAc/petroleum ether) to afford the title compound as a brown solid (0.34 g, 45%): 1H NMR (400 MHz, DMSO-d6) δ 8.45 (m, 1H), 8.24 (m, 1H), 8.04 (m, 2H), 7.01 (m, 1H), 6.17 (d, J=2.1 Hz, 1H), 5.56 (d, J=10.8 Hz, 1H), 4.92 (s, 2H), 4.19 (m, 2H), 1.23 (m, 3H). ESIMS m/z 259.10 ([M+H]+); IR (thin film) 1750, 1660 cm−1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09226500B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-8b6b96daf22d474f85e8cabd6b5b5cae
Quellennotizuspto-grants-2016_01