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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741707Generated: October 26, 2026

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

https://huagongshe.com/reaction/1741707

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 numberUS05334600
Source datasetuspto-grants-1994_08
ORD IDord-1b40f671cefb4b60846d5f217aea54db
Source noteuspto-grants-1994_08