HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-Bromo-4-(1-bromoethyl)-1,3-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl bromide | HCID 68176 | — |
| Reactant | 1-(2-Bromothiazol-4-yl)ethan-1-ol | HCID 66861317 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-4-(1-bromoethyl)-1,3-thiazole | HCID 66860748 | 92.3% |
Reaction Steps
To a stirred solution thionyl bromide (0.787 g, 3.78 mmol, 1.05 eq.) in 20 ml dry DCM, cooled to 5° C., was added dropwise a solution of 1-(2-bromo-1,3-thiazol-4-yl)ethanol (0.75 g, 3.60 mmol, 1 eq.) and pyridine (0.285 g, 3.60 mmol, 1 eq.) in 15 ml dry DCM. On complete addition, the cooling bath was removed, the reaction warmed to room temperature and stirred 1.5 hr. 100 ml of water and 100 ml of DCM were added and stirring allowed for 2 mins. The organic layer was separated, dried of MgSO4 and evaporated to give 2-bromo-4-(1-bromoethyl)-1,3-thiazole (0.9 g, 84% yield) as a yellow viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557849B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-6ae5e7cedafb4a5d9f9efd7e5a21f2fd |
| Source note | uspto-grants-2013_10 |