HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → (S)-N-Cbz-4-methyl-5-oxooxazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | N-carbobenzyloxyalanine | HCID 736104 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (S)-N-Cbz-4-methyl-5-oxooxazolidine | HCID 355115 | 93.4% |
Reaction Steps
Benzyloxycarbonyl-L-alanine (19.3 g), paraformaldehyde (6.56 g) and p-toluenesulfonic acid monohydrate (0.17 g) were suspended in toluene (190 mL), and the mixture was heated at reflux while removing water produced. At the end of the reaction, the reaction mixture was cooled to room temperature, washed with saturated aqueous sodium hydrogen carbonate solution and then saturated saline. The toluene solution was dried over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure, the resulting crystals were filtrated to give the title compound (19.0 g) as white crystals in an yield of 93%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026515B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-e2c0605219b84bff843bba75bf0b3354 |
| Source note | uspto-grants-2006_04 |