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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197806Generated: October 25, 2026

2-Acetylthiophene → Rac-alpha-hydroxy-alpha-propyl-gamma-oxo-2-thiophenebutyric acid

https://huagongshe.com/reaction/1197806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AcetylthiopheneHCID 6920—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Oxovaleric acidHCID 74563—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductRac-alpha-hydroxy-alpha-propyl-gamma-oxo-2-thiophenebutyric acidHCID 5456459741.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05278161
Source datasetuspto-grants-1994_01
ORD IDord-a9394a4307f54d3e8de32a04755f31c9
Source noteuspto-grants-1994_01