HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-bromopropionic acid N-cyano-N-butylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propanoyl bromide, 2-bromo- | HCID 79047 | — |
| Reactant | Butylcyanamide | HCID 12295218 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-bromopropionic acid N-cyano-N-butylamide | HCID 53869097 | 70.8% |
Reaction Steps
29.5 g (0.137 mole) of 2-bromopropionyl bromide are added dropwise at 15° C. to 13.4 g (0.137 mole) of butyl cyanamide and 13.8 g (0.137 mole) of triethylamine in 150 ml of ether. The mixture is stirred for 3 hours at 20° to 25° C., then filtered to remove the precipitated salt. The filtrate is extracted with dilute hydrochloric acid and the extract is dried over sodium sulfate and concentrated by evaporation. The oily residue is distilled under high vacuum, affording 22.6 g (70.8% of theory) of 2-bromopropionic acid N-cyano-N-butylamide with a boiling point of 53°-54° C. at 0.0052 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04759796 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-122e0641a6c54ab6b11527a005f8408d |
| Source note | uspto-grants-1988_07 |