HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2-Chlorocinnamoyl)-3-propyloxyphenethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 2737382 | HCID 2737382 | — |
| Reactant | 103686-13-1 | HCID 15205618 | — |
| Reactant | HCID 22379525 | HCID 22379525 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2-Chlorocinnamoyl)-3-propyloxyphenethylamine | HCID 53771533 | — |
Reaction Steps
To a solution of 2-(3-propyloxyphenyl)ethylamine prepared in a manner analogous to that described in Example 1E (2.69 g) in acetonitrile (40 cm3) was added triethylamine (3 cm3). A solution of 2-chlorocinnamoyl chloride (3.6 g) in acetonitrile (20 cm3) was added slowly, the reaction mixture being cooled in an ice bath. When addition was complete, the mixture was stirred at room temperature for 40 minutes, treated with water (60 cm3) and SVM (2 cm3) and stirred well. The resulting precipitate was filtered off, washed and air-dried (5.49 g) m.p. 96°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04968698 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-e9e8ff2f67384f5b904db53b516dd7c5 |
| Source note | uspto-grants-1990_11 |