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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895783Generated: October 31, 2026

Tributylvinyltin → HCID 67978737, compound

https://huagongshe.com/reaction/1895783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylvinyltinHCID 81998—
Reactant1,1-Dimethylethyl N-[(1R)-1-(3-bromophenyl)ethyl]carbamateHCID 67959607—
CatalystPalladium--triphenylphosphane (1/1)HCID 15220664—
SolventTolueneHCID 1140—
ProductHCID 67978737HCID 6797873782.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of [(R)-1-(3-bromo-phenyl)-ethyl]-carbamic acid tert-butyl ester (10.26 g, 0.0342 mol.) and tributyl(vinyl)stannane (32.5 g, 30 mL, 0.103 mol.) in toluene (175 mL) was purged with nitrogen for 30 minutes before addition of bis(triphenylphosphine palladium II chloride (2.38 g, 0.0034 mol.). The stirred mixture was heated to 60° C. for 16 hours before cooling to room temperature. The reaction mixture was filtered through hyflo-supercel then evaporated to give a dark coloured oil. The oil was purified by silica gel chromatography using iso-hexanes/ethyl acetate 19:1 to yield the title compound (6.95 g, 82%) as a yellow oil. 1H NMR (300 MHz, CDCl3) δ1.39-1.51 (m, 12H), 4.80 (br s, 2H), 5.24-5.32 (m, 1H), 5.77 (d, J=17.6 Hz, 1H), 6.73 (dd, J=17.6, 10.9 Hz, 1H), 7.18-7.36 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513184B2
Source datasetuspto-grants-2013_08
ORD IDord-49ef744f7a674647b180c8b44411cb8f
Source noteuspto-grants-2013_08