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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091798Generated: November 2, 2026

Ethanol → 3-[(8-Chloro-4-oxo-3,4-dihydrophthalazin-1-yl)methyl]benzoic acid

https://huagongshe.com/reaction/1091798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant3-((8-Chloro-4-oxo-3,4-dihydrophthalazin-1-yl)methyl)benzonitrileHCID 57791783—
SolventWaterHCID 962—
Product3-[(8-Chloro-4-oxo-3,4-dihydrophthalazin-1-yl)methyl]benzoic acidHCID 5341603895%

Reaction Conditions

Temperature100 °C

Reaction Steps

3-((8-chloro-4-oxo-3,4-dihydrophthalazin-1-yl)methyl)benzonitrile (117) (3.75 g, 12.68 mmol) and potassium hydroxide (7.11 g, 126.81 mmol) were added to ethanol (30 mL) and water (70 mL) and heated at 100° C. for 5 hours. The ethanol was evaporated off and the aqueous was extracted with ethyl acetate (1×75 mL). The aqueous was then acidified to pH1 with conc HCl to afford a solid, this was filtered, washed with water and dried to afford the desired material as a beige solid (3.81 g, 95% yield); 1H NMR (400.132 MHz, DMSO) δ 4.67 (2H, s), 7.42-7.41 (2H, m), 7.72 (1H, s), 7.79-7.76 (1H, m), 7.81 (1H, t), 7.97 (1H, dd), 8.34 (1H, dd), 12.88 (1H, s); m/z (LC-MS, ESI+), RT=0.92 (M+H 315).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129380B2
Source datasetuspto-grants-2012_03
ORD IDord-87fd6dcf13004886b8f3824580e6d1b9
Source noteuspto-grants-2012_03