HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Bromo-N-(2-(phenylamino)phenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Phenyl-o-phenylenediamine | HCID 68297 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-N-(2-(phenylamino)phenyl)benzamide | HCID 23094055 | 35.4% |
Reaction Steps
To a solution of 4-bromo-benzoyl chloride (11 g, 50 mmol) in anhydrous dichloromethane (DCM) (100 ml), was added N-phenylbenzene-1,2-diamine (10.2 g, 55 mmol), then triethylamine (TEA) (17 ml, 122 mmol) slowly. The whole was stirred at room temperature (RT) overnight. Filtration gave a white solid 1 (6.5 g). The filtrate was worked up with water (300 ml), then extracted with DCM (300 ml) three times. The organic phase was collected and dried over MgSO4, concentrated and recrystallized in DCM/hexanes to give another portion of white solid 1 (10.6 g). Total amount of product 1 is 17.1 g, in 93% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426040B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-bd82fe55b0e24f409130dc3857fccd99 |
| Source note | uspto-grants-2013_04 |