HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-bromo-N-(3-iodophenyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Iodoaniline | HCID 12271 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-bromo-N-(3-iodophenyl)acetamide | HCID 44883470 | 83.1% |
Reaction Steps
To a solution of 3-iodoaniline (2.19 g, 10.0 mmol) and 2-bromoacetyl bromide (0.87 mL, 3.40 g, 10.0 mmol) in DCM (100 mL) was added Et3N (1.39 mL) at 0° C. The reaction mixtures were stirred at room temperature for overnight. The reaction mixtures were diluted with DCM (100 mL), washed with water, and dried over Na2SO4. Solvent was evaporated under reduce pressure to afford a residue, which was purified by biotage eluting with 10% EtOC in hexanes to 100% EtOAc to afford 2-bromo-N-(3-iodophenyl)acetamide (2.824 g, 83%). MS (ESI), 340, 342 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120837B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-4bbd2a986e0e4f2d96fa2b7244dd00d3 |
| Source note | uspto-grants-2015_09 |