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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896043Generated: October 30, 2026

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

https://huagongshe.com/reaction/896043

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, 12.7 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 (0.5M 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 isoquinolin4-yl-acetic acid hydrochloride salt, MH+ 188.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919337B2
Source datasetuspto-grants-2005_07
ORD IDord-d6810b3509d74a6c856a1acfc850c3a5
Source noteuspto-grants-2005_07