HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252070Generated: November 3, 2026
Tributyltin Chloride → HCID 17981611, compound
https://huagongshe.com/reaction/2252070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 2-Methyl-4-phenyl-1,3-thiazole | HCID 584377 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 17981611 | HCID 17981611 | 68% |
Reaction Steps
Add n-butyllithium (0.46 mL, 0.74 mmol, 1.6 M in tetrahydrofuran) to a solution of 2-methyl-4-phenylthiazole (0.13 g, 0.74 mmol) in tetrahydrofuran (7 mL) cooled to −78° C. under a nitrogen atmosphere. Stir at −78° C. for 45 minutes, add tributyltin chloride (0.2 mL, 0.74 mmol), and stir for 2 hours as the reaction mixture warms to room temperature. Add aqueous ammonium chloride and then partition the mixture between ethyl acetate and water. Extract the aqueous phase with ethyl acetate. Wash the combined organic layers sequentially with water and saturated aqueous sodium chloride, dry over sodium sulfate, and concentrate under reduced pressure. Subject the residue to silica gel chromatography, eluting with hexane containing 10% ethyl acetate to provide the desired compound in 68% yield. MS(ES+): m/z=466.1 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07320995B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-c1e81babbb4d4b64ac5ed755ce1e6f5c |
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| Source note | uspto-grants-2008_01 |
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