HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805760Generated: October 31, 2026
Diethyl Ether → 2-[5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propan-2-ol
https://huagongshe.com/reaction/1805760
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Methoxycarbonyl-5-pyridineboronic acid, pinacol ester | HCID 46738663 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]propan-2-ol | HCID 58092932 | — |
Reaction Steps
To a solution of methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinate (Frontier, catalog No. M2012) (1.25 g, 4.75 mmol) in THF (48 mL) was added a solution of methyl magnesium bromide in ethyl ether (3.0 M, 12 mL, 36 mmol) via syringe at 0° C. with an ice water bath under dry N2. The reaction mixture was added at 0° C. for 30 minutes and then the ice-water bath was removed. After stirring at room temperature for 30 minutes, the reaction mixture was poured into saturated NH4Cl solution (300 mL) and followed by addition of 100 mL of EtOAc. The organic phase was separated and the aqueous phase was extracted with EtOAc (2×50 mL). The combined organic phases were washed with brine (10 mL), dried over Na2SO4, and evaporated to afford crude title compound that was used directly in the next step reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354526B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-0dd31a0b154f4e32b008e89dbcdc6af8 |
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| Source note | uspto-grants-2013_01 |
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