HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(6-Bromopyridin-3-yl)ethane-1,2-diol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Ethyl 2-(6-bromopyridin-3-yl)-2-oxoacetate | HCID 46941438 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(6-Bromopyridin-3-yl)ethane-1,2-diol | HCID 46941437 | 77% |
Reaction Steps
To a solution of ethyl (6-bromopyridin-3-yl)(oxo)acetate (1.00 g) in ethanol (20 mL) was slowly added sodium borohydride (250 mg). The reaction mixture was stirred at room temperature for 4 hr, diluted with ethyl acetate and washed with water. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated to give the title compound (650 mg, yield 77%) as a colorless oil. MS: 220 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318746B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-acb1dd40ca2249f98f12b42aa3d02dc3 |
| Source note | uspto-grants-2012_11 |