HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Benzyl-5-(2-nitro-ethyl)-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Benzyl-5-((E)-2-nitro-vinyl)-pyridine | HCID 59255390 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Benzyl-5-(2-nitro-ethyl)-pyridine | HCID 59255135 | 22% |
Reaction Steps
To a mixture of 2-benzyl-5-((E)-2-nitro-vinyl)-pyridine (1.2 g, 5.0 mmol) described in Manufacturing Example 210-1-5, acetic acid (300 mg, 5.0 mmol), and dimethyl sulfoxide (10 mL) was added sodium borohydride (94 mg, 2.5 mmol), which was stirred for 10 minutes at room temperature. The reaction solution was partitioned into ethyl acetate and water. The organic layer was separated and passed through a glass filter provided with NH silica gel (eluted with ethyl acetate). The eluate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=2:1) to obtain the title compound (260 mg, 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841327B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-474e9c06bf91482da949cede5fb24f00 |
| Source note | uspto-grants-2014_09 |