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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389102Generated: October 30, 2026

Chloroform → 1,2,3,4-Tetrahydro-1-oxo-6-isoquinolinecarboxylic acid

https://huagongshe.com/reaction/389102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantPotassium HydroxideHCID 14797—
Reactant1-Oxo-1,2,3,4-tetrahydroisoquinolin-6-YL trifluoromethanesulfonateHCID 53414198—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
Product1,2,3,4-Tetrahydro-1-oxo-6-isoquinolinecarboxylic acidHCID 58243905—

Reaction Conditions

Temperature120 °C

Reaction Steps

Zinc cyanide (744 mg), potassium hydroxide (470 mg) and tetrakis(triphenylphosphine)palladium (0) (1.82 g) were sequentially added to a solution of 1-oxo-1,2,3,4-tetrahydroisoquinolin-6-yl trifluoromethanesulfonate (1.55 g) in NMP (15 ml), followed by stirring at 120° C. for 3 hours. Chloroform was added to the reaction solution, the precipitated solid was separated by filtration, and the solvent of the filtrate was evaporated. The residue was purified by silica gel chromatography (hexane:ethyl acetate=100:0 to 0:100), and the solvent was evaporated under reduced pressure. Subsequently, ethylene glycol (10 ml) and 3M aqueous sodium hydroxide solution (30 ml) were added to the resulting residue, followed by stirring at 100° C. for 3 hours. After cooling to room temperature, water was added thereto, followed by extraction with diethylether. Concentrated hydrochloric acid was added to the aqueous layer, the pH was adjusted to 2 to 3, ethyl acetate was added for re-extraction, the organic layer was washed with saturated brine, and the solvent was evaporated under reduced pressure. Ethyl acetate was added, and the solid was precipitated, filtered and dried under vacuum to obtain, as a colorless solid, 1-oxo-1,2,3,4-tetrahydroisoquinoline-6-carboxylic acid (324 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-4f23b9f681db4e03aa7c2f395aef38d8
Source noteuspto-grants-2013_02