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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296317Generated: November 3, 2026

Tributylvinyltin → HCID 68692187, compound

https://huagongshe.com/reaction/1296317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 68690914HCID 68690914—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 68692187HCID 68692187—

Reaction Conditions

Temperature110 °C

Reaction Steps

Degassed mixture of (R)-2-Benzyl-8-methyl-1,2,3,4,11,11a-hexahydro-pyrazino[1,2-b]isoquinolin-6-one (50 mg, 0.13 mmol), tributyl(vinyl)tin (64 mg, 0.20 mmol), dichlorobis(triphenylphosphine)palladium (9.1 mg, 0.013 mmol) and LiCl (27.5 mg, 0.65 mmol) in toluene (1 mL) was heated at 110° C. for 18 h to give dark brownish reaction mixture. The mixture was then cooled, diluted with ethyl acetate(10 mL) and filtered through bed of celite and rinsed with more ethyl acetate(20 mL). Filtrate was concentrated and purified by prep TLC (SiO2, 95:5, CH2Cl2:MeOH) to give (25 mg, 60%) as a faint yellow oil. MS (ESI) 319 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244843B2
Source datasetuspto-grants-2007_07
ORD IDord-06fd3cc6bdb446afbe53940e30406ffc
Source noteuspto-grants-2007_07