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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1502849Erstellt: 25. Oktober 2026

Sodium Hydroxide → 5-Bromo-3-hydroxyisoindolin-1-one

https://huagongshe.com/reaction/1502849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt4-BromophthalimideHCID 236018—
KatalysatorZincHCID 23994—
KatalysatorCopper sulfate pentahydrateHCID 24463—
Produkt5-Bromo-3-hydroxyisoindolin-1-oneHCID 11615537—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A mixture of Zn powder (1.73 g, 26.154 mmol), copper (II) sulfate pentahydrate (0.02 g, 0.08 mmol) and 2M aq NaOH (27 mL) were cooled to 0° C. 5-Bromoisoindoline-1,3-dione (5 g, 22 mmol) was added at the same temperature over the period of 30 min. The reaction mixture was stirred at 0° C. for 30 min and 3 h at ambient temperature. The reaction mixture was filtered and the filtrate was neutralized with concentrated HCl. The reaction mixture was diluted with ethanol and extracted with ethyl acetate. The combined ethyl acetate layer was dried over Na2SO4 and concentrated under reduced pressure to afford the crude title compound as a brown solid, which was used in the next step without further purification (1.3 g): mp 258-261° C.; 1H NMR (400 MHz, DMSO-d6) δ 9.03 (br, 1H), 7.81 (m, 2H), 7.69 (m, 1H), 6.44 (m, 1H), 5.88 (d, J=9.3 Hz, 1H); ESIMS m/z 225.83 ([M−H]−); IR (thin film) 1684, 3246, 606 cm−1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09211280B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-0a771f2ae1dc40c69355d4edda0cc55b
Quellennotizuspto-grants-2015_12