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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275396Generated: October 30, 2026

Ethanol → HCID 89464205, compound

https://huagongshe.com/reaction/2275396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant6-methoxy-1-methyl-3,4-dihydroisoquinolin-7-olHCID 605698—
ReactantEthylbromopyruvateHCID 21948992—
ProductHCID 89464205HCID 89464205—

Reaction Steps

To a solution of 1-methyl-7-hydroxy-6-methoxy-3,4-dihydroisoquinoline (100 mg) in EtOH (5 ml) was added dropwise under a nitrogen atmosphere ethylbromopyruvate (0.065 ml) and the reaction mixture was heated under reflux for 2 hours. The reaction mixture was allowed to cool to ambient temperature, quenched with a saturated aqueous NaHCO3 solution and extracted with ethyl acetate. The organic layer was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by chromatography on silica gel eluting with heptane and increasing amounts of ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09127007B2
Source datasetuspto-grants-2015_09
ORD IDord-008f0e764baf40209709184e4e89512e
Source noteuspto-grants-2015_09