HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Methoxide → 3-Amino-5-chloro-2-(2-benzyloxybenzoyl)-benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | omega-(2-Cyano-4-chlorophenoxy)-2-benzyloxy-acetophenone | HCID 68535637 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Amino-5-chloro-2-(2-benzyloxybenzoyl)-benzofuran | HCID 11303453 | — |
Reaction Steps
A solution of sodium methanolate (0.07 g, 1.3 mmol) in methanol is added to a solution of ω-(2-cyano-4-chlorophenoxy)-2-benzyloxy-acetophenone (0.5 g, 1.32 mmol) in methanol (30 ml) at 0° C. After 2 h at r.t. the reaction mixture is concentrated under reduced pressure. The residue is diluted with ethyl acetate and washed with water. Drying over sodium sulfate, filtering, evaporating the solvent and purification of the residue by silicagel column chromatography yields the title compound, having a m.p. of 158-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486996B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-798ee60072ea43b882d468c5b9d5ac59 |
| Source note | uspto-grants-2013_07 |