HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylthiophene → Rac-alpha-hydroxy-alpha-propyl-gamma-oxo-2-thiophenebutyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylthiophene | HCID 6920 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Oxovaleric acid | HCID 74563 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Rac-alpha-hydroxy-alpha-propyl-gamma-oxo-2-thiophenebutyric acid | HCID 54564597 | 41.3% |
Reaction Steps
11.2 g (200 mmol) of potassium hydroxide in 75 ml of water are added at 0° dropwise to a suspension of 11.6 g (100 mmol) of 2-oxo-n-valeric acid and 12.6 g (100 mmol) of 2-acetylthiophene in 75 ml of ethanol and the suspension is held at 0° for 48 hours. After evaporation of the ethanol the residue is made acidic with 25% hydrochloric acid and extracted three times with ethyl acetate. The combined ethyl acetate extracts are dried, filtered and evaporated. After chromatography on silica gel using a 5:1 mixture of methylene chloride and methanol as the eluent and crystallisation from ether there are obtained 10.0 g (41%) of rac-α-hydroxy-α-propyl-γ-oxo-2-thiophenebutyric acid as a colorless powder, melting point 128°-131°, MS: 197 (M-COOH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05278161 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-a9394a4307f54d3e8de32a04755f31c9 |
| Source note | uspto-grants-1994_01 |