HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylsulphonyl isocyanate → 1-(4-Bromophenyl)-1-ethyl-3-benzenesulfonylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylsulphonyl isocyanate | HCID 76096 | — |
| Reactant | 4-bromo-N-ethylaniline | HCID 11745656 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Di-n-butyldilauryltin | HCID 9809426 | — |
| Product | 1-(4-Bromophenyl)-1-ethyl-3-benzenesulfonylurea | HCID 12873785 | — |
Reaction Steps
A solution was prepared containing 4.0 g (0.02 mole) of 4-bromo-N-ethylaniline in 25 ml of benzene and one drop each of triethylamine and dibutyltin dilaurate. A solution of 3.7 g (0.02 mole) of benzenesulfonylisocyanate was added to the first solution. The temperature was allowed to rise to 35° C. The mixture was stirred for 2 hours at room temperature and for one-half hour at 40°-45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260824 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-5ec1c9d775ef406da0441c9ab9961a50 |
| Source note | uspto-grants-1981_04 |