HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512160Generated: October 30, 2026
Stannane, tributyl(1-ethoxyethenyl)- → HCID 86716183, compound
https://huagongshe.com/reaction/512160
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | HCID 86716184 | HCID 86716184 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86716183 | HCID 86716183 | 169.8% |
Reaction Steps
A solution of 2-(6-chloropyridin-3-yl)-3-cyclopropylpropanenitrile (1.0 g, 4.86 mmol), tributyl(1-ethoxyvinyl)stannane (3.4 g, 9.72 mmol), Lid (0.612 g, 14.58 mmol) and Pd(PPh3)4 (0.282 mg, 0.243 mmol) in 1,4-dioxane (20 mL) was degassed and heated to 120° C. under N2 overnight. The reaction mixture was diluted with water and extracted with EtOAc (3×30 mL). The combined organic layers were dried over Na2SO4 and concentrated to give 3-cyclopropyl-2-(6-(1-ethoxyvinyl)pyridin-3-yl)propanenitrile (2 g), which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102591B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-18d4a09f42ad4a17ab4664e3b065f363 |
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| Source note | uspto-grants-2015_08 |
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