HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibromomethane → 2-(Phenylthiomethylimino)-1,3-dithietane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,2-Dithietane | HCID 12309283 | — |
| Reactant | Potassium phenylthiomethyldithiocarbamate | HCID 23667329 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Phenylthiomethylimino)-1,3-dithietane | HCID 21453321 | — |
Reaction Steps
To a mixture of 28.2 g. of methylene bromide and 10.9 g. of triethylamine in 250 ml. of dimethylformamide was added, in portions, 27.3 g. of potassium phenylthiomethyldithiocarbamate keeping the reaction temperature below 30°C. by cooling. After another 2 hours, the mixture was poured into water and extracted with ethylene chloride. The ethylene chloride mixture was washed with water, dried, and saturated with dry hydrogen chloride. The resulting salt was collected by filtration and washed with acetone. The salt, on stirring with a mixture of 100 ml. of water and 300 ml. of chloroform, dissolved and removal and concentration of the chloroform layer gave 8.5 g. of the dithietane as a white solid, m.p. 50°-52°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03975528 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-aefb2e0d26a44920833aa411bb07852e |
| Source note | uspto-grants-1976_08 |