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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22192Generated: October 26, 2026

2-Fluorothiophenol → Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate

https://huagongshe.com/reaction/22192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorothiophenolHCID 520216—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 2-(4-fluorophenyl)acrylateHCID 19736751—
SolventEthanolHCID 702—
ProductEthyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetateHCID 1992755282.2%

Reaction Steps

The crude product from Step A (3.9 g, 20 mole) was taken up in 20 ml of ethanol. To this solution, being stirred at room temperature, was added 2-fluorothiophenol (2.5 g, 20 mmole) and 50 mg of solid sodium ethoxide. After stirring for eight hours the ethanol was concentrated and the residue taken up in ether. The ether mixture was washed twice with 15% NaOH solution, dried (MgSO4) and concentrated to a colorless oil (5.3 g, 82% yield). 1H NMR (CDCl3) δ: 7.28 (4H, m), 7.06 (4H, m), 4.13 (2H, m), 3.72 (1H, m), 3.55 (1H, m), 3.20 (1H, dd, J=6, 12 Hz), 1.21 (3H, t, J=6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428027
Source datasetuspto-grants-1995_06
ORD IDord-c5b877e7aced48708173e5628ebd3f82
Source noteuspto-grants-1995_06