HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641087Generated: October 30, 2026
2-(Tributylstannyl)pyridine → HCID 59007746, compound
https://huagongshe.com/reaction/641087
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | HCID 57430841 | HCID 57430841 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59007746 | HCID 59007746 | — |
Reaction Steps
64.8 g (0.26 mol) of 3-(2-chloro-6-fluorophenyl)-2,4,6-trichloropyridine (see Example Ab), 83.6 g (0.29 mol) 2-tri-n-butylstannylpyridine and 4.8 g (5.2 mmol) tetrakistriphenylphosphinepalladium(0), dissolved in 600 ml of dimethylformamide and 400 ml 1,4-dioxane, were boiled under reflux for 8 h and then stirred at room temperature overnight. The volatile components were removed under reduced pressure, and 400 ml of water were then added, the mixture was extracted five times with in each case 150 ml of methyl tert-butyl ether and the combined extracts were washed once with 100 ml of saturated sodium chloride solution, dried over sodium sulfate and concentrated under reduced pressure. The crude product was chromatographed on silica gel using cyclohexane/ethyl acetate and triturated with n-pentane. Yield 36.0 g of a colorless solid of m.p. 45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07695728B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d941eb21b421436eb390320b5cc46d99 |
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| Source note | uspto-grants-2010_04 |
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