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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257051Generated: October 25, 2026

Triethylamine → 3-[2-Benzyl-1-oxo-1,2-dihydroisoquinolin-6-yl]-acrolein

https://huagongshe.com/reaction/257051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcrolein dimethyl acetalHCID 80145—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-Benzyl-6-bromo-isoquinolin-1-oneHCID 18963984—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-[2-Benzyl-1-oxo-1,2-dihydroisoquinolin-6-yl]-acroleinHCID 53919284—

Reaction Steps

A mixture of 2-benzyl-6-bromo-1,2-dihydro-1-oxoisoquinoline (1 g, 3.2 mmol), acrolein dimethyl acetal (2.6 mL, 22.4 mmol), Pd(OAc)2 (15 mg, 0.064 mmol), P(o-tolyl)3 (78 mg, 0.26 mmol) and Et3N (0.5 mL, 3.84 mmol) in DMF (2 mL) is heated in a sealed tube apparatus at 120° for 48 hours. After cooling to room temperature, the reaction mixture is diluted with EtOAc, filtered, washed with saturated NaCl solution, dried over MgSO4 concentrated in vacuo, and the residue is chromatographed (silica gel 1:4 EtOAc/hexane) to yield 3-[2-benzyl-1-oxo-1,2-dihydroisoquinolin-6-yl]-acrolein.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260316
Source datasetuspto-grants-1993_11
ORD IDord-bc6acf83e4354455a1b481c76c067174
Source noteuspto-grants-1993_11