HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)aniline → 4-(4-Trifluoromethylphenylaminosulfonyl)-5-methylisoxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)aniline | HCID 9964 | — |
| Reactant | 5-Methyl-1,2-oxazole-4-sulfonyl chloride | HCID 2776141 | — |
| Reactant | 2-(4-Trifluoromethylphenylaminosulfonyl)1-ethoxypropene | HCID 56982552 | — |
| Product | 4-(4-Trifluoromethylphenylaminosulfonyl)-5-methylisoxazole | HCID 57089194 | — |
Reaction Steps
AA16 was prepared starting from 2-(4-trifluoromethylphenylaminosulfonyl)1-ethoxypropene under the same conditions as described for AA11. Alternatively, AA16 was prepared from 4-trifluoromethylaniline and 4-chlorosulfonyl-5-methylisoxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760066 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-dc4e9641eb91427b9dcb45310c5bab47 |
| Source note | uspto-grants-1998_06 |