Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276101Generated: October 31, 2026

Isoquinoline → Ethyl 1-(2,4,6-trimethylphenyl)-1,2-dihydro-2-isoquinolinecarboxylate

https://huagongshe.com/reaction/276101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoquinolineHCID 8405—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 178425415HCID 178425415—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-(2,4,6-trimethylphenyl)-1,2-dihydro-2-isoquinolinecarboxylateHCID 15895522—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-mesitylmagnesium bromide in THF (1.0 M, 11 mL; 11 mmol) was added to an ice-cold solution of isoquinoline (1.3 g, 10 mmol) in THF (10 ml). After 5 minutes, ethyl chloroformate was added slowly dropwise and the mixture was further stirred at 0° C. for 10 min before quenched by saturated NH4CL solution. The mixture was poured into 0.5 N hydrochloric acid and extracted twice with ethyl ether. Combined organics were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give 3.58 g of titled compound (quantitative) as an oil which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353103B1
Source datasetuspto-grants-2002_03
ORD IDord-c095728ba5b94c78a7f6bb6e6e0451a7
Source noteuspto-grants-2002_03