HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478810Generated: October 31, 2026
Allyltributylstannane → HCID 118513273, compound
https://huagongshe.com/reaction/1478810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-Bromo-4-(trifluoromethoxy)aniline | HCID 688296 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 118513273 | HCID 118513273 | — |
Reaction Steps
To a solution of 2-bromo-4-(trifluoromethoxy)aniline (75 g, 293 mmol) in DMF (1000 ml) was added Pd(PPh3)4 (13.5 g, 11.7 mmol) and allyltributyltin (116 g, 351 mmol) and the reaction mixture was stirred at 80° C. for 16 h. The mixture was cooled to room temperature and saturated aqueous KF solution was added. The mixture was diluted with ethyl acetate (1500 mL) and washed with 1:1 H2O: saturated aqueous NaCl solution (2×750 mL) and saturated aqueous KF (1×). The aqueous layers were combined and extracted with ethyl acetate (250 mL). The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure to give the crude product, which was absorbed onto silica and purified by chromatography eluting with 1% ethyl acetate in petroleum ether to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403833B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-f425d8fc753946928caa289c6725d5a9 |
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| Source note | uspto-grants-2016_08 |
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