HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214667Generated: November 1, 2026
2,4-Difluorobenzaldehyde → 4-Fluoro-2-(methylthio)benzaldehyde
https://huagongshe.com/reaction/2214667
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4-Difluorobenzaldehyde | HCID 73770 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Fluoro-2-(methylthio)benzaldehyde | HCID 21947409 | 75.3% |
Reaction Steps
A suspension of 2,4-difluorobenzaldehyde (16 mL, 146 mmol) and sodium thiomethoxide (14 g, 200 mmol) in toluene (200 mL) was stirred at 80° C. for 7 h and 14 h at room temperature. The reaction mixture was diluted with ether (300 mL), washed with water (100 mL), saturated aqueous NaHCO3 (100 mL) and brine (50 mL). The aqueous layers were combined and extracted with ether (2×100 mL). The organic layers were combined and dried over anhydrous Na2SO4, filtered and concentrated to give a viscous oil. This viscous oil was dissolved in ether/hexanes (1:1, v/v) and slowly concentrated on under vacuum. The precipitated white solid was separated by filteration and dried to give 2-methylthio-4-fluorobenzaldehyde (18.7 g, 75% yield). 1HNMR (500 MHz, CDCl3) δ: 10.11 (1H, s), 7.78 (1H, dd, J=8.55, 6.11 Hz), 6.97 (1H, dd, J=10.07, 2.44 Hz), 6.91 (1H, td, J=8.54, 2.44 Hz), 2.45 (3H, s). MS calcd for C8H7FOS (M+H): 171.2. found: 171.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109186B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-468417d2d2ab4859a7e2640bd9e1ad2d |
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| Source note | uspto-grants-2006_09 |
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