HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301040Generated: October 30, 2026
Tri(butyl)vinyltin → HCID 54535880, compound
https://huagongshe.com/reaction/2301040
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Reactant | HCID 54101286 | HCID 54101286 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 54535880 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498275B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-fd857f975fa24b05b9846ee14ff3f782 |
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| Source note | uspto-grants-2002_12 |
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