HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl isothiocyanate → N-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 3-(Benzyloxy)-5-bromoaniline | HCID 57813626 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-[(3-benzyloxy-5-bromophenyl)carbamothioyl]benzamide | HCID 57813640 | 89% |
Reaction Steps
To a solution of 3-benzyloxy-5-bromo-phenylamine (23.50 g, 84.40 mmol) in acetone (550.0 mL) was added benzoyl isothiocyanate (18.50 mL, 93.13 mmol) and the reaction mixture was stirred at room temperature for 30 min. After the completion of the reaction (TLC monitoring), the solvent was evaporated and the residue thus obtained was washed with hexane to get the desired product (33.0 g, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977340B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-36c4fb42e2de4ff893242813afa30586 |
| Source note | uspto-grants-2011_07 |