HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-sec-BUTYLTHIO-5,7-DINITRO-2-TRIFLUOROMETHYLBENZIMIDAZOLE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Butanethiol | HCID 10560 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-Chloro-5,7-dinitro-2-trifluoromethylbenzimidazole | HCID 135677577 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-sec-BUTYLTHIO-5,7-DINITRO-2-TRIFLUOROMETHYLBENZIMIDAZOLE | HCID 21489379 | — |
Reaction Steps
In 200 milliliters of ethanol, 1 gram of sodium (0.04 mole) was reacted with 3.6 grams of 2-butanethiol (0.04 mole). The mixture was stirred for one-half hour. Then 4-chloro-5,7-dinitro-2-trifluoromethylbenzimidazole (6.2 grams; 0.02 mole) was added, and the resulting reaction mixture was stirred overnight, poured into water, acidified, and filtered to separate the desired 4-sec-butylthio-5,7-dinitro-2-trifluoromethylbenzimidazole. It was recrystallized twice from a mixture of benzene and an aliphatic hydrocarbon fraction boiling at 60°-80° C., m.p., 111°-15° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04000295 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-749beacdde534ab0b2bbb21b806a9724 |
| Source note | uspto-grants-1976_12 |