HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-butanone → 4-Ethyl-2-[2-(4-nitrophenyl)ethyl]-1,3-thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-butanone | HCID 13156 | — |
| Reactant | 3-(4-Nitrophenyl)propanethioamide | HCID 82673146 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-Ethyl-2-[2-(4-nitrophenyl)ethyl]-1,3-thiazole | HCID 69209254 | 95% |
Reaction Steps
A mixture of 3-(4-nitrophenyl)propanethioamide (1.25 g), 1-bromo-2-butanone (0.98 g) and tert-butanol (30 mL) was heated under reflux for 30 min. The reaction mixture was concentrated, and saturated aqueous sodium hydrogen carbonate was added to the residue. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 4-ethyl-2-[2-(4-nitrophenyl)ethyl]-1,3-thiazole as a yellow oil (1.48 g, yield 95%) from a fraction eluted with hexane-ethyl acetate (4:1-2:1, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423159B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-bce00eac5075431fb0aeab203b251a1e |
| Source note | uspto-grants-2008_09 |