HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 3-Phenylsulfanylthiophene-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromothiophene-2-carboxaldehyde | HCID 2797079 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Phenylsulfanylthiophene-2-carbaldehyde | HCID 19780513 | 92% |
Reaction Steps
To a stirred solution of 3-bromothiophene-2-carboxaldehyde (1.9 g, 10 mMol) in ethanol (15 mL) is added thiophenol (2.2 g, 20 mMol) and powdered potassium carbonate (3.04 g, 22 mMol). The mixture is stirred overnight and concentrated. The residue is partitioned between water and ether. The aqueous layer is washed with ether and the organics combined, dried(MgSO4) and concentrated. Purification by flash column (SiO2, eluted with 3% ethylacetate/hexanes) afforded the desired aldehyde (2.02 g, 92%) as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05185363 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-2988e50845fb48159f1867d4c6b5a582 |
| Source note | uspto-grants-1993_02 |