HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413985Generated: October 28, 2026
Formaldehyde → (4S)-N-Boc-4-phenylmethyloxazolidin-5-one
https://huagongshe.com/reaction/413985
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- | HCID 77857 | — |
| Catalyst | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (4S)-N-Boc-4-phenylmethyloxazolidin-5-one | HCID 11482799 | 72.2% |
Reaction Steps
Tert-butoxycarbonyl-L-phenylalanine (20.00 g), paraformaldehyde (6.04 g) and pyridinium p-toluenesulfonate (0.95 g) were added to toluene (200 ml), and they were stirred under heating and reflux for 30 minutes. The reaction mixture was cooled to room temperature and washed with a saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The obtained toluene layer was dried over anhydrous sodium sulfate and then sodium sulfate was removed. The solvent was evaporated under reduced pressure. The concentrated solution was cooled to room temperature to crystallize the product. The crystals were separated and dried to obtain intended (4S)-N-tert-butoxycarbonyl-4-phenylmethyloxazolidin-5-one (15.10 g) (yield: 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06570039B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-481d92e92afd4807b2ac005afe70c119 |
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| Source note | uspto-grants-2003_05 |
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