HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219156Generated: October 25, 2026
Trimethyltin chloride → 2-Methyl-5-(trimethylstannyl)thiazole
https://huagongshe.com/reaction/219156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | 2-Methylthiazole | HCID 77129 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-5-(trimethylstannyl)thiazole | HCID 10264660 | — |
Reaction Steps
Butyllithium (1.6M in THF, 3.5 ml, 5.5 mmol) was added to a stirred solution of 2-methylthiazole (0.45 ml, 5.0 mmol) in THF (15 mL) at −78° C. The reaction mixture was stirred at −78° C. for 40 min. Chlorotrimethylstannane (1M in THF, 5.0 ml, 5.0 mmol) was added. Stirring was continued at −78° C. for 45 min. The reaction mixture was quenched with a satured aqueous solution of NaHCO3. The aqueous layer was extracted with Et2O. The organic extracts were dried over MgSO4, filtered and concentrated in vacuo. Used in the next step without purification (obtained 1.29 g). MS m/z=264.1. Calc'd for C7H13NSSn: 261.94.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198448B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-07d57b1329624653ab2c2de8abb276a4 |
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| Source note | uspto-grants-2012_06 |
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