HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarboxaldehyde → HCID 85446738, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 85446738 | HCID 85446738 | — |
Reaction Steps
About 30 mmol (3.06 g) of 2,5-dihydrothiopnene-1-oxide (MW=102) (4) and 70 mmol=(7.84 g) (6.5ml) of thiophene-2-aldehyde (MW--112, d=1.2 g/cm3) were added to a solution containing 0.9 g of NaOH in 50 ml of H2O and 12.5 ml of tetrahydrofuran. The mixture was stirred for 2 days. Purification was performed by separation by column chromatography; the reaction mixture was applied to a column of silica gel/diethyl ether. The aldehyde was eluted with ether; the product was eluted with ethyl acetate. When the solvent was stripped off in vacuo, the product precipitated. The precipitate was filtered off with suction and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05136049 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-1fbfe1b5e4d14fdeb8d4e8895503830d |
| Source note | uspto-grants-1992_08 |