HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455648Generated: November 1, 2026
Acetone → 2-[5-(Tributylstannyl)-1,3-thiazol-2-yl]propan-2-ol
https://huagongshe.com/reaction/1455648
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Thiazole | HCID 9256 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[5-(Tributylstannyl)-1,3-thiazol-2-yl]propan-2-ol | HCID 46840025 | — |
Reaction Steps
To a solution of thiazole (1.0 eq) in THF (0.2M) at −78° C. was added nBuLi (1.6M, 1.1 eq). After 1 h at −78° C., acetone (1.0 eq) was added and the mixture stirred 30 min at −78° C., 5 min −50° C. then cooled back to −78° C. to add a second equivalent of nBuLi (1.6M, 1.1 eq). After 1.5 h at −78° C., tri-n-butyltin chloride (1.2 eq) was added and the mixture stirred 12 h at −78° C. The reaction mixture was diluted with Et2O and a solution of NH4Cl. The organic extracts were washed with water, brine, dried over MgSO4, filtered and concentrated. Flash chromatography (Hexane:EtOAc, 90:10) afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482456B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-f6ba3af8f1cf4d8f9ace31be503e443d |
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| Source note | uspto-grants-2009_01 |
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