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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372267Generated: October 25, 2026

4-Fluoro-2-methoxybenzonitrile → 4-Fluoro-2-hydroxybenzonitrile

https://huagongshe.com/reaction/1372267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-2-methoxybenzonitrileHCID 2783329—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventTolueneHCID 1140—
Product4-Fluoro-2-hydroxybenzonitrileHCID 1102990195%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of intermediate 127, 4-fluoro-2-methoxybenzonitrile, (4.53 g, 30 mmol;) and AlCl3 (5.0 g, 37.6 mmol; Aldrich) in anhydrous toluene (30 mL) was stirred at approximately 130° C. for 18 hrs. After cooling, ice water (˜50 mL) was added and the resulting mixture extracted with ether (20 mL×2). The combined extracts were washed sequentially with water and brine, then dried (MgSO4), and concentrated in vacuo to provide the title compound (3.90 g, 28.5 mmol, Yield 95%) as a white solid: 1H NMR (DMSO-d6, 300 MHz) δ ppm: 6.74–6.84 (2H, m, Ar—Hs), 7.71 (1H, dd, J=7 Hz, J=8.5 Hz, Ar—H), 11.64 (1H, s, OH); 13C NMR (DMSO-d6, 75.5 Hz) δ ppm: 95.13 102.45, 102.78, 106.53, 106.83 115.53, 134.68, 134.84, 161.41, 161.58, 163.00, 166.35. HRMS (ESI−) calcd for C7H3NOF (M−H) 136.0199. found 136.0199.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157447B2
Source datasetuspto-grants-2007_01
ORD IDord-dbf809677b4549c3b1fb47ef5bcff921
Source noteuspto-grants-2007_01