HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3-Fluoro-4-(methylthio)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3,4-Difluorobenzaldehyde | HCID 588088 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Fluoro-4-(methylthio)benzaldehyde | HCID 11275257 | 61.1% |
Reaction Steps
The 3,4-diflourobenzaldehyde (52.1 g, 0.36 mol) was dissolved in acetonitrile (500 mL). Sodium thiomethoxide (25.6 g, 0.36 mol) was added in four equal portions at 15 minute intervals. The slightly exothermic reaction was stirred at room temperature for 4 hours. The reaction mixture was poured into ethyl acetate (500 mL) and extracted with saturated sodium bicarbonate (2×200 mL) followed by saturated ammounium chloride (2×100 mL). The solution was dried over sodium sulfate and solvent removed at reduced pressure. The 3-flouro-4-(methylthio)-benzaldehyde (38.5 g, 0.22 mol) was isolated by vacuum distillation (135-145° C. at 25 mm Hg) as clear liquid. (61% yield) ESHRMS m/z 171.0302 (calcd for M+H, 171.0280).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06600052B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-f26358b1b0944ce7919d71afb6f9320e |
| Source note | uspto-grants-2003_07 |