HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-Fluoro-4-methoxyphenyl)ethan-1-one → 3-Fluoro-4-methoxy-alpha-oxobenzeneacetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-Fluoro-4-methoxyphenyl)ethan-1-one | HCID 96828 | — |
| Reactant | Oxyselenide | HCID 167175 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Fluoro-4-methoxy-alpha-oxobenzeneacetaldehyde | HCID 12921713 | — |
Reaction Steps
Selenium oxide (4.953 g) is heated to dissolve in 100 ml aqueous dioxane (95:5 dioxane: H2O). The 3-fluoro-4-methoxyacetophenone (5.00 g) is added to the mixture. The resulting mixture is refluxed overnight then coiled. The precipitated selenium metal is filtered. The filtrate is concentrated in vacuo to give a brown thick gum. It is recrystallized from -~200 ml hot H2O, filtered hot and allowed to stand at RT overnight. The precipitated pale pink flake are filtered, washed with H2O and let air dried to give 1-methoxy-2-fluoro-4-glyoxyloylbenzene, which is used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05476851 |
| Source dataset | uspto-grants-1995_12 |
| ORD ID | ord-6bb8e1024614435caf1851fd926bd2a9 |
| Source note | uspto-grants-1995_12 |