HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164516Generated: October 26, 2026
Benzoyl chloride → N-benzoyl-N'-(2-phenoxyphenyl)thiourea
https://huagongshe.com/reaction/1164516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | Benzenamine, 2-phenoxy- | HCID 75899 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-benzoyl-N'-(2-phenoxyphenyl)thiourea | HCID 1488843 | — |
Reaction Steps
To a solution of ammonium thiocyanate (30.2 g) in anhydrous acetone (660 ml) was added dropwise benzoyl chloride (47.6 g) with stirring at 50° C. After refluxing for 1.5 hours, the mixture was cooled to ambient temperature. To the mixture containing benzoyl isothiocyanate was added dropwise a solution of 2-phenoxyaniline (47.6 g) in anhydrous acetone (300 ml). The reaction mixture was refluxed with stirring for 1.5 hours and then concentrated under reduced pressure to give crystals, which were washed twice with water and dried to give crystalline 1-(2-phenoxyphenyl)-3-benzoylthiourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04370340 |
|---|
| Source dataset | uspto-grants-1983_01 |
|---|
| ORD ID | ord-ab736d83e5a04dc182afe110af8bf6be |
|---|
| Source note | uspto-grants-1983_01 |
|---|