HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Bromoacetyl)pyridine hydrobromide → 1,1-Difluoro-1-phenyl-[4-(4-pyridyl)-2-thiazolyl]methane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Bromoacetyl)pyridine hydrobromide | HCID 2776239 | — |
| Reactant | 2,2-Difluoro-2-phenylethanethioamide | HCID 14096960 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,1-Difluoro-1-phenyl-[4-(4-pyridyl)-2-thiazolyl]methane | HCID 14096961 | 48% |
Reaction Steps
To a solution of 2,2-difluoro-2-phenylthioacetamide (1.57 g, 0.0092 mol) in 95% ethanol (20 mL) was added α-bromo-4-acetylpyridine hydrobromide (3.20 g, 0.012 mol) and the mixture warmed on a steam bath for thirty minutes. The product was isolated in the usual way and recrystallized from ethyl acetate/hexane to afford 1,1-difluoro-1-phenyl-[4-(4-pyridyl)-2-thiazolyl]methane (1.27 g, 48%). mp. 54.5°-55.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04725606 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-ee8a5d8d7a7843959078967aa73d7741 |
| Source note | uspto-grants-1988_02 |