HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-[2-(2-chloroethoxy)-phenylsulfonyl]-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 2-(2-Chloroethoxy)benzene-1-sulfonamide | HCID 13729454 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[2-(2-chloroethoxy)-phenylsulfonyl]-N'-methylurea | HCID 20191437 | — |
Reaction Steps
5.9 g of triethylamine is added dropwise to a suspension of 11.0 g of 2-(2-cloroethoxy)-phenylsulfonamide, 50 ml of methylene chloride and 3.3 g of methyl isocyanate within 10 minutes at a temperature of 20°-25° C. The resulting clear solution is stirred for a further hour at room temperature and evaporated to dryness. The residue is solved in 5% aqueous sodium carbonate. After acidification of this solution with 10% hydrochloric acid 12.5 g of N-[2-(2-chloroethoxy)-phenylsulfonyl]-N'-methylurea precipitate therefrom, m.p. 218°-222° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04681619 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-6067e2ba43b74d52b73546aaa39bc53e |
| Source note | uspto-grants-1987_07 |