HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-chloropropane → 2,3,6,7-Tetrahydro-5H-[1,3]thiazolo[2,3-b][1,3]thiazin-4-ium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | 2-Thiazolidinethione | HCID 2723699 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,3,6,7-Tetrahydro-5H-[1,3]thiazolo[2,3-b][1,3]thiazin-4-ium bromide | HCID 21429016 | — |
Reaction Steps
A mixture of 12 g. of thiazolidine-2-thione, and 16 g. of 1-bromo-3-chloro propane in 100 ml. of acetonitrile is refluxed for 12 hours, cooled and the product removed by filtration. Recrystallization from ethanol gives 2,3,5,6-tetrahydrothiazolo[2,3-b]-(1,3)-thiazinium bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962437 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-2c88d7ebca164b9290a79b7c323da0ed |
| Source note | uspto-grants-1976_06 |