HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434126Generated: October 26, 2026
Benzoyl chloride → (S)-3-benzoyl-4-methyl-2,5-oxazolidinedione
https://huagongshe.com/reaction/434126
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | (S)-4-Methyloxazolidine-2,5-dione | HCID 10996998 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-3-benzoyl-4-methyl-2,5-oxazolidinedione | HCID 9855930 | 74% |
Reaction Steps
4-Dimethylaminopyridine (61 mg, 0.5 mmol) and N-methylmorpholine (152 mg, 1.5 mmol) were dissolved in ethyl acetate (15 mL), followed by the addition of (S)-4-methyl-2,5-oxazolidinedione (L-alanine-NCA) (230 mg, 2.0 mmol) under ice cooling. Further, a solution of benzoyl chloride (281 mg, 2.0 mmol) in ethyl acetate (7 mL) was added dropwise under ice cooling over 20 minutes. After the resulting mixture was stirred as was at 0° C. for 2 hours, a precipitated salt was filtered off, and the filtrate was concentrated under reduced pressure. The concentration residue was re-dissolved in a mixed solvent consisting of ethyl acetate (5 mL) and hexane (5 mL), and insoluble matter was filtered off. The filtrate was concentrated under reduced pressure to afford the title compound as white crystals (324 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06670447B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-96b92b1de51b4a06a7c2e328ae01161c |
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| Source note | uspto-grants-2003_12 |
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