HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900705Generated: October 29, 2026
Hydrochloric Acid → 2-(Isoquinolin-4-yl)acetic acid hydrochloride
https://huagongshe.com/reaction/900705
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Isoquinoline | HCID 8405 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | Sodium triethylboranuide | HCID 5129078 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Isoquinolin-4-yl)acetic acid hydrochloride | HCID 69200199 | — |
Reaction Steps
A solution of sodium triethylborohydride (1M THF, 12.7 ml, 12.7 mmol) is added dropwise to a solution of isoquinoline (1.64 g, 12.7 mmol) in THF (25 ml). The reaction is stirred at room temperature for 1 hour, prior to dropwise addition of a solution of ethyl glyoxalate (1.43 g, 13.9 mmol) in toluene (previously heated at 110° C. for 1.5 hours). After a further 4 hours at room temperature, the reaction is cooled to 0° C. and sodium hydroxide (0.5 M aqueous solution, 25.4 ml) followed by hydrogen peroxide (30% aqueous solution, 12.7 ml) is added, followed by stirring for 2 hours. The reaction is acidified with 1N HCl, washed with ethyl acetate three times, the aqueous phase is reduced in volume by evaporation and refrigerated overnight. The resultant precipitate is collected by filtration and dried to afford isoquinolin-4-yl-acetic acid hydrochloride salt, MH+ 188.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07361661B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-2f729cea6b9d4257886ae4988660cb8a |
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| Source note | uspto-grants-2008_04 |
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