HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 6-Bromo-3-pyridinemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Bromo-3-pyridinecarboxaldehyde | HCID 11769234 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-3-pyridinemethanol | HCID 6421249 | 98.5% |
Reaction Steps
To a solution of 4.85 g of 6-bromo-pyridine-3-carboxaldehyde in 50 mL of MeOH at 0° C. was added 1.93 g of NaBH4. This mixture was allowed to warm to room temperature. Upon completion of the reaction, the reaction mixture was concentrated to a residue, which was partitioned between ethyl acetate and water and extracted with ethyl acetate. The organic layer was washed with brine and dried over sodium sulphate. Purification by flash chromatography (silica, heptanes/ethyl acetate) provided 4.83 g of (6-bromo-pyridin-3-yl)-methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919628B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-237772472e3043e1a49f0fd9240e2f53 |
| Source note | uspto-grants-2011_04 |