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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814299Generated: October 31, 2026

Allyltributylstannane → 5-(2-Propen-1-yl)quinoline

https://huagongshe.com/reaction/1814299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyltributylstannaneHCID 90628—
ReactantPotassium FluorideHCID 522689—
Reactant5-BromoquinolineHCID 817321—
SolventTolueneHCID 1140—
Product5-(2-Propen-1-yl)quinolineHCID 2250411095.9%

Reaction Steps

5-Bromo-quinoline (5.6 g, 27 mmol) was dissolved in 40 mL toluene. BHT (50 mg) was added, along with allyl tributyl stannane (9.3 mL, 30 mmol), and tetrakis(triphenyl)phospine palladium (600 mg, 0.52 mmol). The reaction was refluxed overnight, then cooled. Potassium fluoride solution (1.0 g, in 18 mL H2O) was added. The reaction was stirred for 3 hours, then filtered. The reaction mixture was concentrated in vacuo. It was chromatographed in 3:1 hexane/ethyl acetate to yield 4.38 g (95%) of 5-allyl-quinoline as a yellow oil. MS (APCI) m/z 170.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875765B2
Source datasetuspto-grants-2005_04
ORD IDord-57d2c7034a9c4c66b186e7b5d0fbf3e6
Source noteuspto-grants-2005_04