HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927011Generated: October 27, 2026
Pinacol → 5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(tris(propan-2-yl)silyl)-1,3-oxazole
https://huagongshe.com/reaction/927011
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pinacol | HCID 6425 | — |
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | 2-(Tris(propan-2-yl)silyl)-1,3-oxazole | HCID 59596016 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(tris(propan-2-yl)silyl)-1,3-oxazole | HCID 44224311 | — |
Reaction Steps
2-Triisopropylsilanyl-oxazole (intermediate 16, 10 g, 44.365 mmol) is dissolved in 40 mL abs. diethylether under argon. The solution is cooled to −78° C. and n-butyllithium (1.6 M solution in hexane, 100 mL, 160 mmol) is added slowly at that temperature. After stirring for 1 h boronic acid triispropylester (12 mL, 52.193 mmol) 20 mL abs. THF is added slowly. The mixture is stirred for 2 h, and is warmed to r.t. The mixture is quenched with methanol. 2,3-Dihydroxy-2,3-dimethylbutane (pinacole, 5.243 g, 44.365 mmol) is dissolved in 10 mL THF and injected to the mixture at 18° C. within 3 min. The mixture is acidified to pH 5 with acetic acid and stirred for 12 h. After addition of 150 mL diethylether and filtration over silica gel, the solvent is evaporated in vacuo. Yield: 15.2 g; ESI mass spectrum: [M+H]+=352; retention time HPLC: 1.334 min (HPLC method Z001_002).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290457B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-5694f08876f04c02bbc3dbf3333e7005 |
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| Source note | uspto-grants-2016_03 |
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