Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | 3,5-Dibromopyridine | HCID 69369 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1633013-47-4 | HCID 117667452 | 56.5% |
Reaction Steps
To a cooled (−20° C.) solution of 3,5-dibromopyridine (592 mg, 2.5 mmol) in THF (2 mL) is added a solution of isopropylmagnesium chloride-lithium chloride complex in THF (1.7 M, 1.4 mL, 2.4 mmol). The resultant mixture is stirred warming to −10° C. for 30 min. The mixture is recooled to −20° C. and cyclobutanone (230 μL, 3.0 mmol) is added. After stirring for 1 h, the reaction is quenched with saturated aqueous ammonium chloride solution and is extracted with EtOAc. The combined organic extracts are washed with water and brine, dried (MgSO4) and concentrated under reduced pressure. Purification by silica gel column chromatography (0-10% MeOH in DCM) provided 1-(5-bromo-pyridin-3-yl)-cyclobutanol (322 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09181272B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-52a22634602841c2a1f6db7c8875e53e |
|---|
| Source note | uspto-grants-2015_11 |
|---|