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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170081Generated: November 2, 2026

Tributylvinyltin → (2-Methoxy-benzyl)-(5-vinyl-quinolin-2-yl)-amine

https://huagongshe.com/reaction/1170081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant(5-Bromo-quinolin-2-yl)-(2-methoxy-benzyl)-amineHCID 67334552—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product(2-Methoxy-benzyl)-(5-vinyl-quinolin-2-yl)-amineHCID 44218150—

Reaction Steps

(5-Bromo-quinolin-2-yl)-(2-methoxy-benzyl)-amine (1000 mg, 2.92 mmol) was dissolved in 30 mL toluene. The reaction mixture was evacuated and backfilled with argon for three times to remove oxygen. Vinyltributyltin (952 mg, 3.00 mmol) and tetrakis(triphenylphosphine)palladium(0) (67 mg, 0.058 mmol) were added. The reaction mixture was refluxed overnight and evaporated. The residue was poured into 50 mL acetonitrile and extracted three times with heptane (50 mL each) to remove the tin products. The acetonitrile phase was dried with sodium sulfate, filtered and evaporated. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 100:0->80:20 gradient). (2-Methoxy-benzyl)-(5-vinyl-quinolin-2-yl)-amine was obtained as a light yellow gum (544 mg, 64%), MS: m/e=291.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825253B2
Source datasetuspto-grants-2010_11
ORD IDord-df8ac459ebca4fdd9459967ac8475861
Source noteuspto-grants-2010_11