HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromochloromethane → HCID 10241417, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromochloromethane | HCID 6333 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178434161 | HCID 178434161 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10241417 | HCID 10241417 | 91% |
Reaction Steps
To a solution of 2-methyl-1,3,4-thiadiazole-5-thiol (2.64 g : 20 mMol.) in dimethylformamide (40 ml) is added under ice cooling sodium hydride (880 mg : 60% dispersion in oil: 1.1 equivalents : 22 mMol.) in portions, and the mixture is stirred for 10 minutes. To the resulting solution is added bromochloromethane (40 ml), and the mixture is stirred at the same temperature for another 1 hour and 30 minutes. The reaction mixture is diluted with water and extracted with ethyl acetate. The extract is washed with brine, dried over sodium sulfate, and purified by silica gel chromatography (toluene : ethyl acetate=10: 1) to give 5-chloromethylthio-2-methyl-1,3,4-thiadiazole (3.3 g) as colorless oil. Yield: 91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05214037 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-6aca7dfb01004515ba117f79a5242ca5 |
| Source note | uspto-grants-1993_05 |