HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Bromomethyl)-4-(trifluoromethyl)benzene → HCID 18681029, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Bromomethyl)-4-(trifluoromethyl)benzene | HCID 123062 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | N-benzenesulfonyl-4-acetylamino-3-aminobenzamide | HCID 18680999 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18681029 | HCID 18681029 | 40.7% |
Reaction Steps
A methanol (7 ml) solution of N-benzenesulfonyl-4-acetylamino-3-aminobenzamide (0.50 g), 4-(trifluoromethyl)benzyl bromide (0.418 g) and potassium bicarbonate (0.423 g) is stirred for 1 hour at 60° C. to give preliminarily purified N-benzenesulfonyl-4-acetylamino-3-[4-(trifluoromethyl)benzylamino]benzamide (0.30 g). This is dissolved in methanol. When it is left undisturbed crystals precipitated. The crystals are separated through filtration, dried and thus, 6-benzenesulfonylcarbamoyl-2-methyl-1-[4-(trifluoromethyl)benzyl]benzimidazole (0.160 g)is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06348032B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-646eae58c74c434ea18a69879738848e |
| Source note | uspto-grants-2002_02 |