HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(Tributylstannyl)-1,3-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(Tributylstannyl)-1,3-thiazole | HCID 2763259 | 90% |
Reaction Steps
To a mixture of 2-bromothiazole (4.6 mL, 50 mmol) and anhydrous ether (50 mL), there was added an n-BuLi hexane solution (22 mL, 55 mmol) dropwise at −70° C. under nitrogen atmosphere, and the mixture was stirred for 30 minutes. A solution of n-Bu3SnCl (14 mL, 50 mmol) in ether (20 mL) was then added at −70° C., and after stirring for 4 hours, the mixture was raised to room temperature and stirred for another hour. After adding water (50 mL), the organic layer was extracted three times with ether (50 mL), and the solvent was distilled away. It was then purified by silica gel chromatography (hexane:ethyl acetate=20:1) to yield the title compound (17g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569378B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-fca0d3951dc74511af25180362fa3ba4 |
| Source note | uspto-grants-2013_10 |