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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476817Generated: October 30, 2026

Acetic Acid → Ethyl 7-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylate

https://huagongshe.com/reaction/1476817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
ReactantEthyl isocyanoacetateHCID 533707—
ReactantMethyl 5-chloro-2-formylbenzoateHCID 58437623—
SolventDimethylformamideHCID 6228—
ProductEthyl 7-chloro-1-oxo-1,2-dihydroisoquinoline-3-carboxylateHCID 9038685531.8%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred mixture of NaH (1.81 g, 30.3 mmol) in DMF (20 mL) was added a solution of methyl 5-chloro-2-formylbenzoate (5.0 g, 25 mmol) and ethyl 2-isocyanoacetate (2.85 g, 25 mmol) in DMF (60 mL) at 40° C. over a 20 minute period. The reaction mixture was stirred at 20° C. for 2 hours. Its pH was adjusted to 7.0 with acetic acid (10%) and the mixture was extracted with DCM (3×200 mL). The organic layers were combined, washed with brine (200 mL), dried over Na2SO4, and concentrated. The crude product was purified by silica gel column chromatography eluting with petroleum ether and ethyl acetate (PE/EtOAc=15:1-5:1 gradient) to give the title compound (2.0 g, 31%). ESI-MS m/z [M+H]+252.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402841B2
Source datasetuspto-grants-2016_08
ORD IDord-02530edde588415687a8ebb6df7b5fc2
Source noteuspto-grants-2016_08