HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 4-Benzylamino-6-(1,2,2-trichlorovinyl)-1,3-benzenedi-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 4-Bromo-6-trichlorovinyl-1,3-benzenedisulfonamide | HCID 21392435 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Benzylamino-6-(1,2,2-trichlorovinyl)-1,3-benzenedi-sulfonamide | HCID 21392422 | — |
Reaction Steps
A mixture of 0.31 g. of 4-bromo-6-trichlorovinyl-1,3-benzenedisulfonamide and 0.76 ml. of benzylamine is stirred at 100° C for 2 hours and then added to 25 ml. of aqueous acetic acid and cooled in ice. A precipitate is collected by filtration which weighs 0.26 g. after drying, which gives after recrystallization from a ethylacetate/benzene/petroleum benzene mixture 0.17 g. of 4-benzylamino-6-(1,2,2-trichlorovinyl)-1,3-benzenedisulfonamide with m.p. 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064239 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-cd73806467c740338ba7fc85cba59835 |
| Source note | uspto-grants-1977_12 |