HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibromomethane → 2-(p-Chlorophenoxymethylimino)-1,3-dithietane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,2-Dithietane | HCID 12309283 | — |
| Reactant | Potassium p-chlorophenoxymethyldithiocarbamate | HCID 23667330 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(p-Chlorophenoxymethylimino)-1,3-dithietane | HCID 21453282 | — |
Reaction Steps
To a mixture of 19.3 g. of methylene bromide and 3.7 g. of triethylamine in 100 ml. of dimethylformamide was added 10.0 g. of potassium p-chlorophenoxymethyldithiocarbamate in portions. After one to two hours, the mixture was poured into water and partitioned into ethylene chloride. The dried ethylene chloride mixture was saturated with dry hydrogen chloride and the resulting salt collected by filtration. Hydrolysis of the salt in a chloroform-water mixture followed by separation, drying and concentration of the chloroform layer gave 3.5 g. of the dithietane as pale yellow crystals, m.p. 64.5°-66.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04009279 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-04f2db9f073a4161aed49e48dc89dc23 |
| Source note | uspto-grants-1977_02 |