HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357741Generated: October 29, 2026
Water → 5-Methanesulfonylthiophene-2-carboxylic acid
https://huagongshe.com/reaction/357741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 5-(Methylsulfanyl)thiophene-2-carbaldehyde | HCID 2736997 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Solvent | Hydrogen Peroxide | HCID 784 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Methanesulfonylthiophene-2-carboxylic acid | HCID 2740497 | — |
Reaction Steps
5-Methylthio-2-thiophenecarbaldehyde (4.48 g) (synthesized in accordance with the method described in Tetrahydron, 41, 3803 (1985)) was dissolved in acetonitrile (20 ml), and sodium dihydrogen phosphate (1.2 g) in water (10 ml) and 30% aqueous hydrogen peroxide (3.5 ml) were added. Further sodium chlorite (3.85 g) in water (10 ml) was added dropwise under ice-cooling. The mixture was stirred at room temperature for 15 hours, and sodium sulfite (1 g) was added. The mixture was alkalified with 1N aqueous sodium hydroxide and extracted with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-diisopropyl ether to give 5-methanesulfonyl-2-thiphenecarboxylic acid (1.73 g) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05840917 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-b1df5942a1d24aaea02ea1320bbdd56c |
|---|
| Source note | uspto-grants-1998_11 |
|---|