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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170072Generated: October 30, 2026

Styrene → (2-Methoxy-benzyl)-[5-((E)-styryl)-quinolin-2-yl]-amine

https://huagongshe.com/reaction/1170072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStyreneHCID 7501—
ReactantTriethylamineHCID 8471—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant(5-Bromo-quinolin-2-yl)-(2-methoxy-benzyl)-amineHCID 67334552—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(2-Methoxy-benzyl)-[5-((E)-styryl)-quinolin-2-yl]-amineHCID 68433914—

Reaction Conditions

Temperature100 °C

Reaction Steps

(5-Bromo-quinolin-2-yl)-(2-methoxy-benzyl)-amine (200 mg, 0.583 mmol) was dissolved in 3 mL dimethylformamide. Styrene (79 mg, 0.760 mmol), triethylamine (77 mg, 0.760 mmol), tri-o-tolylphosphine (14 mg, 0.046 mmol) and palladium(II)acetate (5 mg, 0.022 mmol) were added. The reaction mixture was stirred in a sealed tube at 100° C. for 2 h. The reaction mixture was poured into 30 mL water and extracted three times with ethyl acetate (30 mL each). The combined organic extracts were dried with sodium sulfate, filtered and evaporated. The residue purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 100:0->80:20 gradient). The title compound was obtained as a light yellow solid (142 mg, 67%),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825253B2
Source datasetuspto-grants-2010_11
ORD IDord-35e7f1c343af4c4b80203ffb32c8ed19
Source noteuspto-grants-2010_11