HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → N-{2-Nitro-4-[(1,3-thiazol-2-yl)sulfanyl]phenyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Thiocyanic acid, 4-(acetylamino)-3-nitrophenyl ester | HCID 8180927 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-{2-Nitro-4-[(1,3-thiazol-2-yl)sulfanyl]phenyl}acetamide | HCID 21482791 | — |
Reaction Steps
To a solution of 2.37 g. of 1-acetamido-2-nitro-4-thiocyanatobenzene in 10 ml. dimethylformamide, there is added under nitrogen at less than 30° C., 0.38 g. of sodium borohydride. The mixture is stirred at 20°-30° C. for 1 hour, then 3.2 ml. of 2-bromothiazole is added. The mixture is heated to 130°-135° C. for 1 hour, then cooled and diluted with water. The crude product is filtered off and recrystallized from methanol yielding 1-acetamido-2-nitro-4-(thiazol-2-ylthio)benzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005202 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-69be1e57efb341669dc6bbdf412d4473 |
| Source note | uspto-grants-1977_01 |