HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → HCID 21433227, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | HCID 21433224 | HCID 21433224 | — |
| Product | HCID 21433227 | HCID 21433227 | — |
Reaction Steps
2-Amino-4-trifluoromethyl-5-bromo-benzenesulfonamide (formula (V): R2 = Br) is first prepared according to the above-described technique. M.p.= 202° C. The 2-amino-4-trifluoromethyl-5-bromobenzenesulfonamide (9.60 g) is then reacted, as in Example 2A, with p-anisic acid chloride (6.8 g), to give 12.2 g 2-p-anisoylamino-4-trifluoromethyl-5-bromo-benzenesulfonamide, M.p.= 321° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04025508 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-9cb1bd12b84343c8a2309c37984764f9 |
| Source note | uspto-grants-1977_05 |