HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197565Generated: October 31, 2026
Tributyltin Chloride → HCID 58207969, compound
https://huagongshe.com/reaction/2197565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 58207984 | HCID 58207984 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58207969 | HCID 58207969 | 40.3% |
Reaction Steps
LDA (0.55M 1.1 mmol, 2M) was added to a RBF containing THF (5 mL) cooled to −78° C. A solution of tert-butyl isopropyl(thiazol-2-yl)carbamate (242 mg, 1 mmol) in THF (5 mL) was added via cannula and the resulting solution stirred for 2 h at −78° C. Tributyltin chloride (0.27 mL, 1 mmol) was added and the reaction mixture allowed to slowly warm to room temperature then stirred overnight. The reaction mixture was then quenched with NH4Cl (2 mL, sat. aq.) and diluted with water. The mixture was then extracted with EtOAc (3×25 mL) and the combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo. The product was isolated via column chromatography (SiO2, 2% EtOAc/heptane) to afford the product (214 mg, 40% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338604B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-6eabc2831afa4512abae137fc07d6d33 |
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| Source note | uspto-grants-2012_12 |
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