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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373966Generated: October 31, 2026

Sodium thiocyanate → 2-(4-Fluorophenyl)acetyl isothiocyanate

https://huagongshe.com/reaction/2373966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium thiocyanateHCID 516871—
Reactant4-Fluorophenylacetyl chlorideHCID 3744988—
SolventEthyl AcetateHCID 8857—
Product2-(4-Fluorophenyl)acetyl isothiocyanateHCID 23153248—

Reaction Steps

4-Fluorophenylacetylchloride (Aldrich, 0.072 mL, 0.525 mmol, 2.5 eq) was added to a solution of sodium thiocyanate (0.056 g, 0.695 mmol, 3.3 eq) in ethyl acetate (2.0 mL) at room temperature and the reaction mixture was stirred for 1.5 h to afford a solution of 2-(4-fluorophenyl)ethanoyl isothiocyanate (0.263 M). A solution of 4-(2-chloropyridin-4-yloxy)-3-fluorobenzenamine (0.050 g, 0.21 mmol, 1.0 eq) in CH2Cl2 (1.0 mL) was added dropwise to the 2-(4-fluorophenyl)ethanoyl isothiocyanate solution and the reaction mixture was stirred at room temperature for 12 h. The reaction mixture was concentrated in vacuo and the resulting residue was purified by silica gel flash chromatography (Merck, 40-63 μM, 230-240 mesh, eluting 3/1 hexane/ethyl acetate) to afford the title compound (0.058 g, 64%) as a solid. 1H NMR (DMSO-d6) δ 12.46 (s, 1H), 11.84 (s, 1H), 8.35-8.33 (m, 1H), 8.02-8.33 (m, 1H), 6.99-7.52 (m, 8H), 3.84 (s, 2H); MS(ESI+) m/z 434 (M+H)+; HRMS(ESI+) calcd.: 434.0542, found: 434.0547.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459562B2
Source datasetuspto-grants-2008_12
ORD IDord-cb67560fec5041f0a8c4c98a754c5370
Source noteuspto-grants-2008_12