HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989860Generated: October 31, 2026
Tributyltin Chloride → HCID 22631811, compound
https://huagongshe.com/reaction/989860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 22631972 | HCID 22631972 | — |
| Reactant | LiHMDS tetrahydrofuran | HCID 23714775 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22631811 | HCID 22631811 | — |
Reaction Steps
A 1.59 N n-butyl lithium/n-hexane solution (0.189 ml) was added dropwise at −73° C. in an argon atmosphere to a solution of 66.5 mg of 7-phenylthioimidazo[5,1-b]thiazole in 3 ml of THF. Subsequently, 0.098 ml of tri-n-butylstannyl chloride was added to the mixture. The mixture was stirred at the same temperature for 15 min. The temperature of the system was raised to −40° C. A 1.0 N lithiumbis(trimethylsilyl)amide/THF solution (0.11 ml) was added thereto. The mixture was stirred for one hr. An aqueous ammonium chloride solution was added to the reaction solution. The mixture was extracted with ethyl acetate. 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 115 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-b551b982bf7241158a50b96dfa82b2aa |
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| Source note | uspto-grants-2002_10 |
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