HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478877Generated: October 26, 2026
Tributylstannane → HCID 10992697, compound
https://huagongshe.com/reaction/478877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | (2E)-3-Methyl-2-penten-4-yn-1-ol | HCID 5367604 | — |
| Reactant | Ammonium chloride ammonium hydroxide | HCID 21863491 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10992697 | HCID 10992697 | — |
Reaction Steps
CuCN (2.01 g, 22.40 mmol) is introduced into a round-bottomed flask placed under argon, THF (60 ml) is then added and the mixture is cooled to −78° C. n-Butyl-lithium (1.6M, 27.7 ml, 44.40 mmol) is then added drop-wise and the mixture is allowed to slowly return to room temperature. It is again cooled to −78° C. and n-Bu3SnH (12 ml, 44.40 mmol) is added and the mixture is stirred for minutes, during which the hydrogen is discharged (2E)-3-Methylpent-2-en-4-yn-1-ol (1.86 g, 19.31 mmol) is then added, the reaction mixture is left stirring for 45 minutes and then poured into 200 ml of an NH4OH/NH4Cl (10/90) solution. Extraction is carried out with ether (3×100 ml), drying is carried out over Na2SO4 and evaporation is carried out under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06642273B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-d348f861ebb64f3eb3abec0274e7a36d |
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| Source note | uspto-grants-2003_11 |
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