HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-oxo-4-(2-oxo-1-pyrrolidinyl)butanoyl]-L-prolinol → (4-oxo-4-(2-oxo-pyrrolidinyl)butanoyl]-L-prolinal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-oxo-4-(2-oxo-1-pyrrolidinyl)butanoyl]-L-prolinol | HCID 54104429 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (4-oxo-4-(2-oxo-pyrrolidinyl)butanoyl]-L-prolinal | HCID 86745882 | — |
Reaction Steps
N-[(4-Oxo-4-(2-oxo-1-pyrrolidinyl)butanoyl]-L-prolinol (105 mg) was dissolved in a mixed solvent of benzene (0.25 ml), DMSO (0.79 ml) and triethylamine (0.25 ml), and sulfur trioxide pyridine complex (285 mg) was added thereto under ice-cooling. After 0.5 hour's stirring at a temperature of 10°-15° C., the reaction mixture was poured into ice water, and extracted with chloroform. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate and saturated brine in sequence. The organic layer was dried over magnesium sulfate, followed by concentration. The residue was purified by PLC (chloroform:methanol=49:1) using silica gel to give 65 mg of N-[(4-oxo-4-(2-oxo-pyrrolidinyl)butanoyl]-L-prolinal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05118811 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-99ebea4a52144c5bb9e094b635724f1d |
| Source note | uspto-grants-1992_06 |