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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357536Generated: October 31, 2026

Potassium Hydroxide → 3-(1-(Isopropylamino)phthalazin-6-yl)-4-methylbenzoic acid

https://huagongshe.com/reaction/2357536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 3-(1-(isopropylamino)phthalazin-6-yl)-4-methylbenzoateHCID 68453005—
SolventWater ethanolHCID 19096565—
Product3-(1-(Isopropylamino)phthalazin-6-yl)-4-methylbenzoic acidHCID 68455653—

Reaction Steps

A stirred solution of ethyl 3-(1-(isopropylamino)phthalazin-6-yl)-4-methylbenzoate (4 g, 11 mmol) (obtained by method D below) in ethanol/water (4:1) (50 mL) at RT was treated with potassium hydroxide (1 g, 23 mmol). The mixture was warmed to reflux and stirred for 2 h (M+1=322). The mixture was cooled to RT, then concentrated to remove the organic solvent. The mixture was diluted with 1 N aq. sodium hydroxide (20 mL), extracted with ether (2×50 mL). The combined ether extract was washed with 1N aq. sodium hydroxide (20 mL). The combined water layer was neutralized to pH 7 with conc. HCl. The white precipitate was collected and washed with water (20 mL), azotropically dried with toluene and placed under high vacuum to give 3-(1-(isopropylamino)phthalazin-6-yl)-4-methylbenzoic acid as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-13ea86d2a6c24dc0b731d4bff8c3b6d7
Source noteuspto-grants-2010_07