HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 5-Bromo-2-((triisopropylsilyloxy)methyl)thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triisopropylsilyl chloride | HCID 139400 | — |
| Reactant | (5-Bromo-1,3-thiazol-2-yl)methanol | HCID 11953783 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Bromo-2-((triisopropylsilyloxy)methyl)thiazole | HCID 86695418 | 104% |
Reaction Steps
A 100 mL round bottom flask is charged with (5-bromothiazol-2-yl)methanol (2.5 g, 12.9 mmol), imidazole (1.75 g, 25.8 mmol), dimethylformamide (25 mL), and chlorotriisopropylsilane (3.4 mL, 15.5 mmol). The reaction is stirred at room temperature under nitrogen for 72 hours. Contents are diluted with ethylacetate (150 mL), washed with 0.5M hydrochloric acid (2×100 mL) and brine (100 mL), dried (Na2SO4), and concentrated under vacuum to afford the title compound (4.7 g): m/z (Cl) M+H 350+352.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340564B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-d2e18e2e7bbe4b16ab4610f73556121f |
| Source note | uspto-grants-2016_05 |