HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 5-[2-(methylsulfinyl)phenyl]-1H-pyrrole-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-[2-(methylthio)phenyl]-1H-pyrrole-3-carbaldehyde | HCID 86630988 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-[2-(methylsulfinyl)phenyl]-1H-pyrrole-3-carbaldehyde | HCID 86630990 | 75% |
Reaction Steps
To a solution of 5-[2-(methylthio)phenyl]-1H-pyrrole-3-carbaldehyde (200 mg) in ethyl acetate (10 mL) was added 3-chloroperbenzoic acid (238 mg) under ice-cooling. After stirring at room temperature for 1 hr, a saturated sodium thiosulfate aqueous solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:ethyl acetate) to give the title compound as a pale-pink powder (yield 160 mg, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07977488B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-239ab026d69c48c28a8c1d6947d52ad8 |
| Source note | uspto-grants-2011_07 |