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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745805Generated: November 1, 2026

Hydrochloric Acid → 2-(Isoquinolin-4-yl)acetic acid hydrochloride

https://huagongshe.com/reaction/1745805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantIsoquinolineHCID 8405—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl oxoacetateHCID 70211—
ReactantSodium triethylboranuideHCID 5129078—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product2-(Isoquinolin-4-yl)acetic acid hydrochlorideHCID 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. 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 (0.5M 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019136B2
Source datasetuspto-grants-2006_03
ORD IDord-06a1d40670b146b7af66e3191e3903b0
Source noteuspto-grants-2006_03