HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triisopropylsilyl chloride → HCID 90303362, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triisopropylsilyl chloride | HCID 139400 | — |
| Reactant | HCID 90303529 | HCID 90303529 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90303362 | HCID 90303362 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
At −78° C., a soln. of n-BuLi in hexanes (2.18 M, 16.7 mL, 36.4 mmol) was added over 30 min to a soln. of 5-bromo-4-(oxiran-2-ylmethoxy)thiazole (7.17 g, 30.4 mmol) in THF (564 mL). The mixture was stirred at −78° C. for 2 h, then, TIPSCl (6.63 mL, 31.0 mmol) was added, the mixture was allowed to warm to RT and stirred at RT for 30 min. Subsequently, the mixture was cooled to −78° C. and treated with a soln. of n-BuLi in hexanes (2.18 M, 13.9 mL, 30.4 mmol). The mixture was stirred at 0° C. for 2 h, then, it was quenched with aq. sat. NaHCO3 and extracted with EtOAc. The comb. org. layers were washed with brine, dried over MgSO4, and conc. in vacuo. The residue was purified by means of CC (5-50% EtOAc/Hept) to provide a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388198B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-d52183082f014c9a8a15766da8102e46 |
| Source note | uspto-grants-2016_07 |