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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237188Generated: November 1, 2026

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

https://huagongshe.com/reaction/2237188

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 numberUS07714138B2
Source datasetuspto-grants-2010_05
ORD IDord-847e8bbd110a4ed885b840a5e56a4a16
Source noteuspto-grants-2010_05