HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 21660613, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 69084075 | HCID 69084075 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21660613 | HCID 21660613 | — |
Reaction Steps
A solution of methyl 6-(thiazol-2-yl)picolinate (230 mg; 1.04 mmol) in anh. EtOH (3 ml) was treated with NaBH4 (197 mg; 5.22 mmol), and the resulting mixture was stirred at rt, under nitrogen, for 17 h. After concentration to dryness under reduced pressure, the resulting residue was treated with water, and extracted with DCM. The organic layer was then dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by FC (DCM/MeOH=25/1) afforded (6-(thiazol-2-yl)pyridin-2-yl)methanol as an orange solid. LC-MS (conditions A): tR=0.45 min.; [M+H]+: 193.05 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242970B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-9f2965db760f476aa85d4bfd83d1c236 |
| Source note | uspto-grants-2016_01 |