HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dibromoethane → 2-(2-Bromoethylthio)-4,5-bis-(p-methoxyphenyl)-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | 4,5-Bis-(p-methoxyphenyl)-thiazoline-2-thione | HCID 13209656 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-(2-Bromoethylthio)-4,5-bis-(p-methoxyphenyl)-thiazole | HCID 20458330 | — |
Reaction Steps
2.0 g of 4,5-bis-(p-methoxyphenyl)-thiazoline-2-thione are dissolved in 10.4 ml of 2 N sodium hydroxide solution. 2.3 g of dibromoethane are added and the mixture is stirred at room temperature for 4 hours. The organic layer is then removed, the aqueous phase is subsequently shaken with 10 ml of toluene, and the combined organic phases are washed twice with 5 ml of 2 N sodium hydroxide solution each time, dried over magnesium sulphate and concentrated to dryness by evaporation under reduced pressure. 2-(2-Bromoethylthio)-4,5-bis-(p-methoxyphenyl)-thiazole, Rf =0.65 (silica gel, toluene/ethyl acetate 10:1) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04451471 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-04306c8c39a9436798350f8b937568aa |
| Source note | uspto-grants-1984_05 |