HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 19608684, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 19608716 | HCID 19608716 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 73630007 | HCID 73630007 | — |
| Product | HCID 19608684 | HCID 19608684 | 26% |
Reaction Steps
3-(3-Chloro-4-methoxyphenyl)-5-methyl-4-[4-(methylthio)phenyl]isoxazole was prepared in 26% yield from 1-(3-chlori-4-methoxyphenyl)-2-[4-(methylthio)phenyl]-ethan-1-one oxime from Step 5 and acetic anhydride by the method described in Example 4, Step 1 and then oxidized to 3-(3-chloro-4 methoxyphenyl)-5-methyl-4-[4-methylsulfonylphenyl]isoxazole with Oxone® by the method described in Example 5, Step 4: Mass spectrum: MLi+=384. High resolution mass spectrum calc'd. for C18H17ClNO4S (M+H): 378.0567. Found: 378.0573.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859257 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-3abd5edad4194a6db3ba0e00d74e07c6 |
| Source note | uspto-grants-1999_01 |