HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-Benzyl-5-(N,N-dimethylthiocarbamoyl)thio-4-isothiazolin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-benzyl-5-chloroisothiazol-3(2H)-one | HCID 4345152 | — |
| Reactant | Sodium dimethyldithiocarbamate dihydrate | HCID 23693613 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Benzyl-5-(N,N-dimethylthiocarbamoyl)thio-4-isothiazolin-3-one | HCID 12852727 | 60% |
Reaction Steps
To a solution of 6.76 g. (0.03 mole) of 2-benzyl-5-chloro-4-isothiazolin-3-one in 25 ml of ethanol was added a solution of 5.37 g. (0.03 mole) of N,N-dimethyldithiocarbamic acid sodium salt dihydrate in 30 ml of ethanol followed by 0.1 g. of sodium iodide. A yellow solid separated spontaneously. The mixture was stirred at room temperature for 3 hours, then cooled and filtered. The solid was triturated with 50 ml of water and recrystallized from 250 ml of boiling EtOH to give 5.6 g. (60% yield) of the named product, mp 184°-186°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310590 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-7418178551d446d4aeac9a32f44bb6f8 |
| Source note | uspto-grants-1982_01 |