HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → (S)-3-(3-phenylpropanoyl)-4-methyl-2,5-oxazolidinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Benzenepropanoyl chloride | HCID 64801 | — |
| Reactant | (S)-4-Methyloxazolidine-2,5-dione | HCID 10996998 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-3-(3-phenylpropanoyl)-4-methyl-2,5-oxazolidinedione | HCID 59119731 | 55% |
Reaction Steps
(S)-4-methyl-2,5-oxazolidinedione (L-alanine-NCA) (345 mg, 3 mmol) was dissolved in ethyl acetate (20 mL), followed by the addition of 3-phenylpropanoyl chloride (658 mg, 3.9 mmol) under ice cooling. Further, a solution of N-methyl-morpholine (394 mg, 3.9 mmol) in ethyl acetate (10 mL) was added dropwise under ice cooling over 20 minutes, and the resulting mixture was then stirred at the same temperature for 2 hours. The reaction mixture was treated in a similar manner as in Synthesis Process 5 of Example 8 to afford the title compound (408 mg, 55%) as a colorless clear syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06670447B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-e4d415af27a24464a60ad98809652090 |
| Source note | uspto-grants-2003_12 |