HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Phenylalanine → 5-Benzyl-3-(2,5-difluorophenyl)imidazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Difluoro-2-isocyanatobenzene | HCID 2733266 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Benzyl-3-(2,5-difluorophenyl)imidazolidine-2,4-dione | HCID 14650505 | 82.8% |
Reaction Steps
2,5-Difluorophenylisocyanate (1.55 g, 10.0 mmol) in methylene chloride (25 mL) was added dropwise to a suspension of phenylalanine (1.65 g, 10.0 mmo) in methylene chloride (50 mL) containing triethylamine (1.4 mL, 1.01 g, 10.0 mmol). The solution was allowed to stir overnight, and was then concentrated. The residue was taken up into 6N HCl and heated to reflux for 3 hours. The cooled solution was extracted with ethyl acetate (3×), and the combined extracts where washed with water (2×), dried (over MgSO4), filtered and concentrated to give 2.7 grams. Purification by column chromatography gave 2.5 grams of 5-benzyl-3-(2,5-difluorophenyl)imidazolidine-2,4-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04911748 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-f4788d490a2d48f7b3a07ec54118ddb7 |
| Source note | uspto-grants-1990_03 |