HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444294Generated: October 30, 2026
1,2-Dibromoethane → HCID 13526427, compound
https://huagongshe.com/reaction/444294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178503124 | HCID 178503124 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13526427 | HCID 13526427 | — |
Reaction Steps
A mixture of 19.5 g. (0.06 mole) of 4,5-bis-(p-methylthiophenyl)-2-mercaptoimidazole, 10.7 g. (0.06 mole) of 1,2-dibromoethane and 7.9 g. (0.06 mole) of potassium carbonate in dimethylformamide (250 ml.) was refluxed for 3 hours. The mixture was then poured into 1 liter of ice-water and the yellow precipitate collected and washed with water. This material was then dissolved in chloroform, dried over magnesium sulfate, filtered and the solvent removed at reduced pressure. The residue was then treated with chloroform-ether and the white crystals of 5,6-bis(p-methylthiophenyl)-2,3-dihydroimidazo[2,1-b]thiazole collected. This was then dissolved in methanol and treated with aqueous hydrobromic acid. Filtering and recrystallizing from methanol gave 5,6-bis(p-methylthiophenyl)-2,3-dihydroimidazo[2,1-b]thiazole hydrobromide, m.p. 270° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04263311 |
|---|
| Source dataset | uspto-grants-1981_04 |
|---|
| ORD ID | ord-1a11c80a071f450d8d20f9f7b9b00603 |
|---|
| Source note | uspto-grants-1981_04 |
|---|