HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483589Generated: October 26, 2026
Thiazole → 2-(Trimethylstannyl)-1,3-thiazole
https://huagongshe.com/reaction/483589
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiazole | HCID 9256 | — |
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(Trimethylstannyl)-1,3-thiazole | HCID 12956641 | 71.7% |
Reaction Steps
To 99.99 ml of n-butyl lithium in hexane, dissolved in 200 ml of ether is added dropwise with stirring over 1 hour, at -78° C., a solution of 16 g of thiazole in 100 ml of ether over 1 hour. A solution of 49.81 g of trimethyltin chloride in 100 ml of ether is added dropwise over 20 minutes followed by additional stirring for 1 hour. The reaction mixture is poured into saturated sodium bicarbonate and the organic layer separated, dried and evaporated to a residue. The residue is vacuum distilled to give 33.4 g of the desired product as a colorless liquid, B.P. 60°-65° C./0.7 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225425 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-822f84c084bc4c9c879b6f2fdfdec1c0 |
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| Source note | uspto-grants-1993_07 |
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