HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → 4-Oxazolidinecarboxaldehyde, 3-acetyl-2,2-dimethyl-5-[4-(methylthio)phenyl]-, (4S-cis)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Oxazolidinecarboxaldehyde, 3-acetyl-2,2-dimethyl-5-[4-(methylthio)phenyl]-, (4R-trans)- | HCID 11055477 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Oxazolidinecarboxaldehyde, 3-acetyl-2,2-dimethyl-5-[4-(methylthio)phenyl]-, (4S-cis)- | HCID 11055476 | — |
Reaction Steps
Pyrrolidine (9.6 mg; 0.065 mmol) was added at 25° C. to a solution of compound 4 (see example 3) (100 mg, 0.34 mmol) in toluene (2 ml) kept under magnetic stirring and under nitrogen. At the end of the addition the mixture was kept at 25° C. under stirring for 14 hours. The reaction mixture was then poured into 10% NaHCO3 ; after separation of the phases, the aqueous phase was extracted with CH2Cl2. The combined organic phases were dried over sodium sulphate and evaporated to dryness under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05401852 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-5863f01b06da4a8996052eb6e1254ff2 |
| Source note | uspto-grants-1995_03 |