HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196871Generated: October 31, 2026
Bromochloromethane → HCID 10241417, compound
https://huagongshe.com/reaction/1196871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromochloromethane | HCID 6333 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | HCID 178434161 | HCID 178434161 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10241417 | HCID 10241417 | 164.4% |
Reaction Steps
2-Mercapto-5-methyl-1,3,4-thiadiazole (41.4 g, 313 mmol) was added to an ice-bath cooled (5° C.) aqueous solution of 85% KOH (20.7 g, 313 mmol) in EtOH (160 mL). The ice bath was removed and the mixture stirred until complete dissolution occurred (30 min). The solvent was then evaporated to leave a viscous oil which solidified. The resulting potassium salt was dissolved in CH3CN (200 mL), and the solution was cooled in an ice bath and treated with bromochloromethane (121 g, 939 mmol). The ice in the bath was allowed to melt and the mixture was further stirred at R.T. for 25 h. The reaction mixture was partitioned between EtOAc and H2O. The organic phase was dried (MgSO4) and evaporated. The residue was purified by passing through a pad of silica gel, eluted first with CH2Cl2 and then with 5% CH3CN/CH2Cl2 to afford 93.0 g (76.0%) of 2-[(chloromethyl)-thio]-5-methyl-1,3,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05116833 |
|---|
| Source dataset | uspto-grants-1992_05 |
|---|
| ORD ID | ord-6a96135823de435d8d6e3fcbd2206951 |
|---|
| Source note | uspto-grants-1992_05 |
|---|