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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 220264Erstellt: 24. Oktober 2026

Trimethyl phosphite → 3-(Isoquinolin-4-yl)acrylic Acid t-Butyl Ester

https://huagongshe.com/de/reaction/220264

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethyl phosphiteHCID 8472—
Edukttert-Butyl acrylateHCID 15458—
Edukt4-BromoisoquinolineHCID 73743—
EduktDiisopropylethylamineHCID 81531—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(Isoquinolin-4-yl)acrylic Acid t-Butyl EsterHCID 68414460—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a mixture of 3 g of 4-bromoisoquinoline, 6.2 mL of acrylic acid tert.-butyl ester and 2.66 mL of DIPEA in 30 mL of DMF under argon was added 0.169 mL of P(OMe)3 and 160 mg of Pd(OAc)2. The reaction mixture was heated for 2 h at 120° C. and the DMF was evaporated under vacuo. The resulting residue was diluted with DCM and filtered over a pad of silica gel. The filtrate was washed with 10%-citric acid, water and brine. The organic phase was dried over anh. Na2SO4 and concentrated in vacuo. The resulting crude material was purified by CC using heptane/EtOAc from 94/6 to 50/50 as eluant to yield 2.7 g of 3-isoquinolin-4-yl-acrylic acid tert.-butyl ester as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202885B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-0de19a722697466aa16e3b3efa644e10
Quellennotizuspto-grants-2012_06