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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427766Generated: November 2, 2026

Tributylvinyltin → HCID 86675861, compound

https://huagongshe.com/reaction/1427766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant(1R)-1-(3-bromophenyl)ethan-1-olHCID 2734889—
CatalystHCID 178418476HCID 178418476—
SolventTolueneHCID 1140—
ProductHCID 86675861HCID 8667586189%

Reaction Conditions

Temperature45 °C

Reaction Steps

Bis(triphenylphosphine)palladium(II) dichloride (360 mg, 0.512 mmol) was added to a degassed solution of (R)-1-(3-bromo-phenyl)-ethanol (1.03 g, 5.123 mmol) and tributyl(vinyl)tin (1.8 ml, 6.15 mmol) in toluene (10 ml) under N2 and the reaction was stirred at 45° C. for 18 h. Tributyl(vinyl)tin (2.56 mmol, 750 uL) and bis(triphenylphosphine)palladium(II) dichloride (0.256 mmol, 180 mg) were added and stirring was continued for 18 h. The reaction was cooled and the solvent evaporated to afford a residue which was absorbed onto SiO2. Purification by SiO2 (3:11-hexane/ethyl acetate) afforded 13a as a yellow oil (675 mg, 89%). 1H NMR (300 MHz, CDCl3) δ7.49 (1H, s), 7.33 (3H, m), 6.75 (1H, dd, J=17.6, 10.9 Hz), 5.80 (1H, d, J=17.6 Hz), 5.28 (1H, d, J=10.7 Hz), 4.93 (1H, m), 1.81 (1H, d, J=3.1 Hz), 1.52 (3H, d, J=6.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933015B2
Source datasetuspto-grants-2015_01
ORD IDord-2473b59140e249b0913a7089a4a6b8dd
Source noteuspto-grants-2015_01