HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 2-bromo-N-(2,2,3,3,3-pentafluoropropyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 2,2,3,3,3-Pentafluoropropylamine | HCID 79002 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-bromo-N-(2,2,3,3,3-pentafluoropropyl)acetamide | HCID 59456546 | 101.4% |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
2,2,3,3,3-Pentafluoropropylamine (produced by Synquest) (389 g) was dissolved in ethyl acetate (1.56 L), and N,N-dimethylaniline (316 g) was added thereto. After cooling the mixture to −10° C., bromoacetyl bromide (500 g) was added dropwise thereto, and the resulting mixture was stirred at a temperature between 10° C. and 0° C. for 2 hours. The organic layer was sequentially washed with aqueous hydrochloric acid, aqueous sodium bicarbonate and with brine, and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure to obtain 2-bromo-N-(2,2,3,3,3-pentafluoropropyl)acetamide (678 g) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08212059B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-1aada4678f73404c993a2f0c0f107ab6 |
| Source note | uspto-grants-2012_07 |