HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-[2-(2-chloroethoxy)-phenylsulfonyl]-N'-methylurea → 2-(2-Chloroethoxy)benzene-1-sulfonyl isocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-[2-(2-chloroethoxy)-phenylsulfonyl]-N'-methylurea | HCID 20191437 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2-(2-Chloroethoxy)benzene-1-sulfonyl isocyanate | HCID 19418414 | 98.4% |
Reaction Steps
12.5 g of N-[2-(2-chloroethoxy)-phenylsulfonyl]-N'-methylurea are suspended in 210 ml of chlorobenzene. This suspension is dried by azeotropic destilling off 20 ml of the solvent. 7.0 g of phosgene are introduced into the reaction mixture within 45 minutes at a temperature of 120°-130° C. Evaporation to dryness of the resulting clear solution yields 11.0 g of 2-(2-chloroethoxy)-phenylsulfonyl isocyanate in form of a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04514212 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-a741d98c4758435086ef2f026f79328b |
| Source note | uspto-grants-1985_04 |