HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → N-(4-bromo-2-methylthiazol-5-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | N-(2-Methylthiazol-5-yl)acetamide | HCID 73554716 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Sodium Bisulfite | HCID 23665763 | — |
| Product | N-(4-bromo-2-methylthiazol-5-yl)acetamide | HCID 86715559 | 67% |
Reaction Steps
To a solution of N-(2-methylthiazol-5-yl)acetamide (0.4 g, 2.6 mmol) in CHCl3 (30 mL) was added Br2 (0.15 mL, 2.8 mmol), then the solution was stirred at room temperature for 12 h to give a brown solution. The reaction mixture was diluted with saturated NaHSO3 solution. The aqueous layer was extracted with DCM (3×30 mL). The combined organic layers were dried with Na2SO4, filtered and concentrated to afford a yellow solid. The resulting mixture was deposited onto silica gel and loaded onto a silica gel column and eluted with PE/EA(1:1) to give the title compound (400 mg, yield 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388180B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-432fd5a06d8249868afbdf458b1a3e7c |
| Source note | uspto-grants-2016_07 |