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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618270Generated: October 30, 2026

Potassium Hydroxide → 4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/1618270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acid benzyl esterHCID 66713169—
SolventEthanolHCID 702—
Product4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acidHCID 6671289290.2%

Reaction Steps

A mixture of 4-Benzyloxy-1-methoxymethyl-isoquinoline-3-carboxylic acid benzyl ester (198 mg, 0.48 mmol), KOH (325 mg, 5 mmol) and EtOH (10 ml) was stirred at ambient temperature for 18 h before the solvent was evaporated in vacuo. To the residue was added water (25 ml) and the mixture was washed with Et2O (2×25 ml). Then the solution was acidified by addition of aqueous 6N HCl and extracted with EtOAc (25 ml). The organic phase was dried over MgSO4 and concentrated in vacuo to give the title compound as a yellow oil (140 mg); MS-(+)-ion: M+1=324.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765956B2
Source datasetuspto-grants-2014_07
ORD IDord-af3d31f6efa64ac2a22ec197ba9c2a41
Source noteuspto-grants-2014_07