Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196871Generated: October 31, 2026

Bromochloromethane → HCID 10241417, compound

https://huagongshe.com/reaction/1196871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromochloromethaneHCID 6333—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassiumHCID 5462222—
ReactantHCID 178434161HCID 178434161—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
ProductHCID 10241417HCID 10241417164.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116833
Source datasetuspto-grants-1992_05
ORD IDord-6a96135823de435d8d6e3fcbd2206951
Source noteuspto-grants-1992_05