HuagongsheHuagongshe Chemistry Print Report · For research reference only
benzyl [(1S,2R)-2-hydroxy-1-methyl-2-pyridin-4-ylethyl]carbamate → 4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | benzyl [(1S,2R)-2-hydroxy-1-methyl-2-pyridin-4-ylethyl]carbamate | HCID 86630532 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | KOH MeOH THF | HCID 86630533 | — |
| Product | 4-Methyl-5-phenyl-2-oxazolidinone, (4S,5R)- | HCID 853161 | — |
Reaction Steps
A solution of benzyl [(1S,2R)-2-hydroxy-1-methyl-2-pyridin-4-ylethyl]carbamate in 7.5N aq. KOH/MeOH/THF (1:2:4, 7 mL) was stirred at room temperature overnight. The reaction was diluted with water (20 mL) and extracted with EtOAc (3×20 mL). The combined organic layers were dried (Na2SO4) and concentrated in vacuo to afford (4S,5R)-4-methyl-5-phenyl-1,3-oxazolidin-2-one. LCMS calc.=179.1; found=179.2 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915271B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-92002cf8bdbf4bab969061a72a7d691b |
| Source note | uspto-grants-2011_03 |