HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269655Generated: October 25, 2026
Sodium Hydroxide → 2-(Isoquinolin-5-yloxy)acetic acid
https://huagongshe.com/reaction/2269655
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 5-isoquinolyloxyacetate | HCID 453435 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Isoquinolin-5-yloxy)acetic acid | HCID 12902790 | 85% |
Reaction Steps
To an ice-cooled solution of 29.0 g of 5-hydroxyisoquinoline in 300 ml of DMF, 11.0 g of sodium methylate was added portionwise. After stirring for 30 min, 17.9 ml of methyl chloroacetate was added dropwise, and the resultant mixture was stirred at room temperature overnight and concentrated under reduced pressure. To the residue, 300 ml of toluene and 300 ml of water were added, and the whole mixture was filtered. The aqueous layer was extracted with 50 ml of toluene, and the combined toluene solution was treated with 2 g of charcoal and evaporated to give methyl 5-isoquinolyloxyacetate. The ester was dissolved in 100 ml of methanol, reacted with 80 ml of 3 N sodium hydroxide aqueous solution for 30 min. The reaction mixture was concentrated under reduced pressure, diluted with 80 ml of water and 160 ml of acetone, and neutralized with 20 ml of concentrated hydrochloric acid. The precipitates formed were filtered, washed with 80 ml of 50% aqueous acetone, and dried to give 34.5 g (85% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329502B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-0803cefbf1224737913d547511c8eed7 |
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| Source note | uspto-grants-2001_12 |
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