HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Bromo-N-(5-methyl-isoxazol-3-yl)-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 3-Amino-5-methylisoxazole | HCID 66172 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-N-(5-methyl-isoxazol-3-yl)-acetamide | HCID 6485065 | — |
Reaction Conditions
| Temperature | -40 °C |
|---|
Reaction Steps
To a stirred solution of 5-methyl-isoxazol-3-ylamine (4.0 g, 40.8 mmol) and triethylamine (6.8 ml, 50 mmol) in chloroform (20 ml) cooled to −40° C., is added bromoacetyl bromide (3.9 ml, 44.9 mmol) in chloroform (20 ml). The reaction mixture is stirred at −40° C. for 30 minutes and then allowed to warm to room temperature. The resultant suspension is filtered, washed with DCM and dried in vacuo to yield the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07723356B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-e1cfa6179eae4288a4def748a48c1cf0 |
| Source note | uspto-grants-2010_05 |