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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 3-(1-(isopropylamino)phthalazin-6-yl)-4-methylbenzoate | HCID 68453005 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 3-(1-(Isopropylamino)phthalazin-6-yl)-4-methylbenzoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759337B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-13ea86d2a6c24dc0b731d4bff8c3b6d7 |
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| Source note | uspto-grants-2010_07 |
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