HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → N-(4-Ethylbenzoyl)phenylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | D-Phenylalanine | HCID 71567 | — |
| Reactant | 4-Ethylbenzoyl chloride | HCID 85368 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | N-(4-Ethylbenzoyl)phenylalanine | HCID 129105 | 84.1% |
Reaction Steps
D-Phenylalanine 2 g (12 mmole) was dissolved in 10% aqueous sodium hydroxide solution (10 ml), and acetone (10 ml) was added. An acetone (5 ml) solution of 4-ethyl benzoyl choride (2.5 g, 15 mmole) and a 10% aqueous sodium hydroxide solution were added dropwise to the mixture obtained above while stirring and cooling with ice over 20 minutes, the reaction solution being maintained at pH 10. The reaction solution was returned to the room temperature, stirred for 3 hours, and made an acidic with a dilute hydrochloric acid solution to precipitate crystals. The crystals were filtered, washed with water and recrystallized from ethyl acetate to obtain N-(4-etylbenzoyl)-D-phenylalanine (3.0 g, yield 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816484 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-4fb4a73965744606861db76598c60f0a |
| Source note | uspto-grants-1989_03 |