HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470483Generated: November 3, 2026
Potassium Hydroxide → 5-Bromoisoquinoline-4-carboxylic acid
https://huagongshe.com/reaction/1470483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 5-bromoisoquinoline-4-carboxylate | HCID 68281832 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromoisoquinoline-4-carboxylic acid | HCID 68281923 | — |
Reaction Steps
To a stirred solution of methyl 5-bromoisoquinolin-4-carboxylate (Intermediate-16) (10.1 g, 38.0 mmol) in MeOH (50 mL) was added, KOH (21.3 g, 380 mmol) dissolved in water (50 mL) and the reaction mixture was heated to 70° C. for 3 h. Then it was concentrated, diluted with water and washed with Et2O (100 mL×3). The aqueous layer was acidified with 2N HCl (pH=3) and the white solid obtained was filtered to yield the desired acid derivative 6.0 g (62.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006442B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-f1868970be9448e6984a1bf06e3ae4ea |
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| Source note | uspto-grants-2015_04 |
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