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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301040Generated: October 30, 2026

Tri(butyl)vinyltin → HCID 54535880, compound

https://huagongshe.com/reaction/2301040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri(butyl)vinyltinHCID 53438229—
ReactantHCID 54101286HCID 54101286—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 54535880HCID 54535880—

Reaction Steps

Tributylvinyltin (0.28 ml) was added to a deoxygenated suspension of (R)-N-[2-bromo-4-(4-mesylphenylsulphonyl)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide (Example 140) (0.50 g) and tris(dibenzylideneacetone)dipalladium(0) (0.05 g) in anhydrous toluene (10 ml). The mixture was heated under reflux with stirring. After 14 hours a further portion of tris(dibenzylideneacetone)dipalladium(0) (0.05 g) and tributylvinyltin (0.28 ml) was added and heating was continued for a further 7 hours. The reaction mixture was allowed to cool and volatile materials were removed by evaporation. The residue was purified on a silica gel Mega Bond Elut column eluting with 5-50% ethyl acetate/hexane to give the title compound (0.146 g) as a solid. NMR (CDCl3) 1.74 (s, 3H), 3.06 (s, 3H), 5.65-5.82 (dd, 2H), 6.67-6.77 (dd, 1H), 7.86-7.89 (dd, 1H), 7.95 (s, 1H), 8.06-8.16 (m, 4H), 8.35 (d, 1H), 8.79 (s, 1H); MS (ESP−): 477.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498275B1
Source datasetuspto-grants-2002_12
ORD IDord-fd857f975fa24b05b9846ee14ff3f782
Source noteuspto-grants-2002_12