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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406482Generated: October 26, 2026

Ethyl iodoacetate → (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/406482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl iodoacetateHCID 12183—
ReactantSodium hydrideHCID 24758—
Reactant3,4-dihydroisoquinolin-1(2H)-oneHCID 150896—
SolventTolueneHCID 1140—
Product(1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl esterHCID 59764846—

Reaction Steps

To a solution of 3,4-dihydro-2H-isoquinolin-1-one (0.250 g, 1.70 mmol) in toluene (5 mL) was added sodium hydride (60% in mineral oil, 0.049 g, 2.04 mmol) and the resulting suspension was heated at about reflux for about 1 h. The reaction mixture was cooled at room temperature and ethyl 2-iodoacetate (0.364 g, 1.70 mmol) was added dropwise and the mixture was again heated at about reflux for about 12 h. The reaction mixture was cooled at room temperature and filtered, rinsed with toluene. The filtrate was concentrated in vacuo to provide (1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-acetic acid ethyl ester as a peach oil (0.336 g, 1.44 mmol). The crude material was used in subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754107B2
Source datasetuspto-grants-2014_06
ORD IDord-1d1de92b70de414f8fecb0ebfe936e74
Source noteuspto-grants-2014_06