HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-(2-Benzoyl-4-chlorophenyl)-1-methyl-3-phenylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | 2-(Methylamino)-5-chlorobenzophenone | HCID 13925 | — |
| Product | 1-(2-Benzoyl-4-chlorophenyl)-1-methyl-3-phenylurea | HCID 23471628 | 66% |
Reaction Steps
A solution of 12.3 g (0.05 mole) of 5-chloro-2-methylaminobenzophenone and 11.9 g (0.1 mole) of phenyl isocyanate in 50 ml of methylene chloride was refluxed for 3 days, and then evaporated to dryness under reduced pressure. The residual syrup was stirred with ether until it crystallized. The crystals were collected on a filter and washed with ether to give 12.06 g (66%) of 1-(2-benzoyl-4-chlorophenyl)-1-methyl-3-phenylurea as light yellow crystals. A sample was recrystallized from ethanol to give colorless crystals: mp 158°-160°; 1H nmr (DMSO-d6) δ3.41 ppm (s, 3H), 6.7-7.5 ppm (m, 13H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04258187 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-c800b6ad2fc14cb9906fc0dc171e83fc |
| Source note | uspto-grants-1981_03 |