HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-[4-(6-Bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | ethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetate | HCID 59525977 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[4-(6-Bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]ethanol | HCID 59526312 | — |
Reaction Steps
To a solution of NaBH4 (60 mg, 1.58 mmol) in MeOH (3.0 mL) at room temperature was added ethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetate (245 mg, 0.79 mmol) in MeOH (7.0 mL) The reaction was stirred at room temperature for 2 h. It was then diluted with water and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered, and evaporated. Flash chromatography (20-100% EtOAc/hexanes) afforded the title compound as a colorless gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367706B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-37c3845d1eeb4d459582c137cdd8120d |
| Source note | uspto-grants-2013_02 |