HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 6-Chloro-1-ethyl-2-methyl-7-methylamino-5-trifluoromethylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 6-Chloro-1-ethyl-2-methyl-5-(trifluoromethyl)-1H-benzimidazol-7-amine | HCID 14281419 | — |
| Product | 6-Chloro-1-ethyl-2-methyl-7-methylamino-5-trifluoromethylbenzimidazole | HCID 21540601 | 73.3% |
Reaction Steps
To 1.0g. of 7-amino-6-chloro-1-ethyl-2-methyl-5-trifluoromethylbenzimidazole (Example IV) dissolved in 10 ml. of concentrated H2SO4 was added 1.0g. of paraformaldehyde. The resultant mixture was stirred at 80°C. for 2 hours and then poured onto ice. The resultant brown solution was made basic by addition of concentrated NH4OH, precipitating a light brown solid. The mixture was extracted with chloroform and the chloroform extracts washed with water and dried over Na2SO4. After removal of the chloroform by evaporation, the residue was extracted with hexane and the hexane extract distilled to dryness. The solid residue was recrystallized from hexane to give 0.77g. (73.3%) of the desired product, m.p. 116.5°-119°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03954438 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-9fd6e9933156497cab8477bb0f19bbc1 |
| Source note | uspto-grants-1976_05 |