HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Benzyloxy-5-(2-nitro-ethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(Benzyloxy)-5-[(E)-2-nitroethenyl]pyridine | HCID 56605146 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Benzyloxy-5-(2-nitro-ethyl)pyridine | HCID 59255069 | 43% |
Reaction Steps
To a solution of 2-benzyloxy-5-((E)-2-nitro-vinyl)-pyridine (5.80 g, 22.8 mmol) described in Manufacturing Example 12-1-3 and acetic acid (5.80 mL) in dimethyl sulfoxide (70 mL) was added sodium borohydride (1.44 g, 36.2 mmol) under nitrogen atmosphere at room temperature while cooling appropriately, which was stirred for 10 minutes at room temperature. The reaction mixture was partitioned into water and ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:4) to obtain the title compound (2.50 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153662B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-cfdf117d7759474c8240ca99f8763cec |
| Source note | uspto-grants-2012_04 |