HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → N-(2,4,6-tribromophenyl)-N'-(p-toluenesulfonyl) urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,4,6-Tribromoaniline | HCID 8986 | — |
| Reactant | o-Toluenesulfonyl Isocyanate | HCID 2733313 | — |
| Product | N-(2,4,6-tribromophenyl)-N'-(p-toluenesulfonyl) urea | HCID 14388505 | — |
Reaction Steps
50 mmol of 2,4,6-tribromoaniline were dissolved in 20 ml of tetrahydrofuran. A solution of 50 mmol of toluenesulfonyl isocyanate in 20 ml of tetrahydrofuran was added dropwise at room temperature, and the stirred reaction mixture was subsequently kept at 40° C. for 3 hours. The precipitated crystals were filtered off under suction. After recrystallization from toluene, the product had a melting point of 230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05403697 |
| Source dataset | uspto-grants-1995_04 |
| ORD ID | ord-a60a42da56dc4ca5aada36d5eefc0806 |
| Source note | uspto-grants-1995_04 |