HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989854Generated: November 1, 2026
Tributyltin Chloride → HCID 23448993, compound
https://huagongshe.com/reaction/989854
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 23449105 | HCID 23449105 | — |
| Reactant | LiHMDS tetrahydrofuran | HCID 23714775 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 23448993 | HCID 23448993 | — |
Reaction Steps
7-t-Butyldimethylsilyloxyacetyl-5-methylimidazo-[5,1-b]thiazole (49.5 mg) was dissolved in 2 ml of THF and 0.4 ml of HMPA. Tri-n-butylstannyl chloride (0.059 ml) and 0.319 ml of a 1.0 N lithiumbis(trimethylsilyl)amide/THF solution were added dropwise in that order to the solution in an argon atmosphere at −73° C. The mixture was stirred at the same temperature for one hr. A 1.0 N lithiumbis(trimethylsilyl)amide/THF solution (0.160 ml) was added dropwise thereto. The mixture was stirred at the same temperature for additional 40 min. An ammonium chloride solution was added to the reaction solution, followed by extraction with ethyl acetate and washing three times with brine. The extract was dried over anhydrous magnesium sulfate and then filtered. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1) to give 66.9 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458780B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-5848c8289d624f3388f5b58fb61b2e32 |
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| Source note | uspto-grants-2002_10 |
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