HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293693Generated: October 31, 2026
5-Methyl-2-thiophenecarboxaldehyde → α-Ethyl-5-methyl-2-thiophenemethanol
https://huagongshe.com/reaction/2293693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Methyl-2-thiophenecarboxaldehyde | HCID 61663 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | α-Ethyl-5-methyl-2-thiophenemethanol | HCID 19780497 | — |
Reaction Steps
5-Methyl-2-thiophenecarboxaldehyde (10.0 g) is dissolved in THF and cooled to -78° C. To that solution is added ethyl magnesium bromide (1M in hexane; 80 cc) dropwise over several minutes. The cooling bath is removed and the reaction allowed to equilbrate to room temperature. The reaction is quenched by adding a saturated solution of NH4Cl. The reaction is extracted with ether, dried and evaporated to yield the title product as an almost colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05686486 |
|---|
| Source dataset | uspto-grants-1997_11 |
|---|
| ORD ID | ord-4da02d2d385c45558367a1a3bafe7b48 |
|---|
| Source note | uspto-grants-1997_11 |
|---|