HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloromethyl phenyl sulphide → 2-Phenylthiomethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloromethyl phenyl sulphide | HCID 81623 | — |
| Reactant | 4-Propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide | HCID 18922253 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Phenylthiomethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide | HCID 19424449 | 88% |
Reaction Steps
A mixture of 4-propyl-5-methyl-1, 2,5-thiadiazolidin-3-one 1,1-dioxide (9 g) , phenylthiomethyl chloride (7.43 g) and tetrabutylammonium bromide (1 g) was suspended in 200 ml of toluene, refluxed for 8 hours, cooled, and concentrated in vacuo. The residue was purified by flash chromatography (15-20% ethyl acetate in hexane) to afford 8.5 g (88%) of 2-phenylthiomethyl-4-propyl-5-methyl-1,2,5-thiadiazolidin-3-one 1,1-dioxide (Formula VI: R1 =H; R2 =propyl; R3 =CH3) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05494925 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-7052a37f66f1443399e412d8aa6fe661 |
| Source note | uspto-grants-1996_02 |