Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793194Generated: October 27, 2026

Allyltributylstannane → 5-Allylisoquinoline

https://huagongshe.com/reaction/1793194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyltributylstannaneHCID 90628—
ReactantPotassium FluorideHCID 522689—
Reactant5-BromoisoquinolineHCID 736487—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTolueneHCID 1140—
Product5-AllylisoquinolineHCID 2202596392%

Reaction Steps

5-Bromoisoquinoline (Preparation 6, Step 1, 1.04 g, 5.0 mmol) was mixed with allyltributyltin (1.7 mL, 5.5 mmol) and dichloropalladium bis(triphenylphosphine) (176 mg, 0.25 mmol) in toluene (20 mL) under a nitrogen atmosphere. The mixture was heated at reflux for 16 h. After cooling to room temperature, a saturated aqueous solution of potassium fluoride (20 mL) was added with stirring, resulting in the formation of a precipitate. Following 15 min of stirring, the mixture was filtered and the organic layer was separated from the aqueous layer, was concentrated in vacuo and was purified by silica gel chromatography (6:1 hexanes-ethyl acetate) to give 778 mg (92% yield) of 5-allylisoquinoline; 1H NMR (400 MHz, CDCl3) δ 9.25 (s, 1H), 8.54 (d, J=5.8 Hz, 1H), 7.85 (m, 1H), 7.79 (d, J=5.8 Hz, 1H), 7.56 (m, 2H), 6.1 (m, 1H), 5.15 (m, 1H), 5.05 (m, 1H), 3.81 (d, J=6.2 Hz, 2H); MS (AP/CI): 170.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078529B2
Source datasetuspto-grants-2006_07
ORD IDord-45852c4d4052420286b592d39aa1fdb0
Source noteuspto-grants-2006_07