HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous Chloride → HCID 88201970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | HCID 88201839 | HCID 88201839 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 88201970 | HCID 88201970 | 100% |
Reaction Steps
A mixture of isomer A of 4-methoxyphenyl 3-nitrophenyl ketone O-benzyloxime (974 mg) [prepared as described in step (a) above] and tin (II) chloride (2.55 g) in ethanol (30 ml) was heated under reflux for 1 hour. After removal of the ethanol by evaporation, the residue was diluted with ethyl acetate. The ethyl acetate was washed with a 5N aqueous solution of sodium hydroxide, with water and then with a saturated aqueous solution of sodium chloride. It was then dried over anhydrous magnesium sulfate and evaporated under reduced pressure, to afford isomer A of the title compound (893 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329405B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-8ecd02f7a4d84de8acf034e81907a62e |
| Source note | uspto-grants-2001_12 |