HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Methyl 4-(2-formylphenylthio)butyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | Methyl 4-sulfanylbutanoate | HCID 11332495 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-(2-formylphenylthio)butyrate | HCID 11413730 | 95% |
Reaction Steps
Under an argon atmosphere, 2-fluorobenzaldehyde (3 g) was dissolved in 9 ml of dimethylformamide and potassium carbonate (5.01 g) was added. Methyl 4-mercaptobutyrate (4.5 ml) was added at room temperature and-was stirred at room temperature for 14 hours. After the addition of 50 ml of ethyl acetate, the mixture was washed with 30 ml of water twice, 3 ml of a 1N hydrochloric acid, and 30 ml of water three times. After drying with anhydrous sodium sulfate, the mixture was concentrated. The concentrated matter was subjected to silica gel chromatography (hexane/ethyl acetate=6/1) purification. The resulting effective fractions were concentrated to yield methyl 4-(2-formylphenylthio)butyrate (5.45 g, Yield 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06566535B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-49e61231f5be4cec897988809330f817 |
| Source note | uspto-grants-2003_05 |