HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-Benzyloxy-3-(2-nitro-ethyl)-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Benzyloxy-trans-beta-nitrostyrene | HCID 5368282 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-Benzyloxy-3-(2-nitro-ethyl)-benzene | HCID 59255205 | 57% |
Reaction Steps
To an acetic acid (5.5 mL) and dimethyl sulfoxide (94 mL) solution of 1-benzyloxy-3-((E)-2-nitro-vinyl)-benzene (5.5 g, 21.5 mmol) described in Manufacturing Example 61-1-2 was added sodium borohydride (1.3 g, 34.4 mmol) at room temperature while cooling appropriately. This mixture was stirred for 1.5 hours at room temperature. This mixture was partitioned into ethyl acetate and water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=10:1-4:1) to obtain the title compound (3.14 g, 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691882B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-f3312406b5254db9a4b4b5865306b900 |
| Source note | uspto-grants-2010_04 |