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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874777Generated: November 1, 2026

Hydrochloric Acid → HCID 25158671, compound

https://huagongshe.com/reaction/1874777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant1,2,3-Trifluoro-4-nitrobenzeneHCID 69871—
Reactant3-Chloro-5-hydroxybenzonitrileHCID 21949878—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 25158671HCID 2515867174.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Chloro-5-hydroxybenzonitrile (20.0 g, 130 mmol) was dissolved in anhydrous THF (500 mL) and cooled to 0° C. Sodium hydride (60% dispersion in oil, 4.81 g, 125 mmol) was added and stirred for 30 minutes. 2,3,4-Trifluoronitrobenzene (23.06 g, 130 mmol) was added and the reaction was allowed to warm to RT. Stirring was continued until TLC showed no remaining starting material. The reaction mixture was poured into a mixture of 10% HCl and ice. Ethyl acetate was added and the organic layer was separated, dried over MgSO4, filtered and evaporated. The resulting oil was triturated with hexanes and Et2O to afford a solid. The washing were collected, evaporated and triturated with hexanes. The materials were combined to afford the title compound (30 g, 74%) as a solid. 1H NMR (400 MHz, CDCl3): δ ppm 7.98 (ddd, 1H), 7.43 (t, 1H), 7.34 (ddd, 1H), 7.21 (t, 1H), 7.08 (dd, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-6bf55c538e60475eaf765cd0fe044d1e
Source noteuspto-grants-2012_11