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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228642Generated: October 30, 2026

Acetonitrile → 4-Bromo-2-hydroxybenzonitrile

https://huagongshe.com/reaction/2228642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium HydroxideHCID 14798—
Reactant18-Crown-6HCID 28557—
ReactantPotassium AcetateHCID 517044—
Reactant5-Bromo-2-fluorobenzonitrileHCID 2724900—
Product4-Bromo-2-hydroxybenzonitrileHCID 1296696181%

Reaction Steps

A mixture of 2-fluoro-5-bromobenzonitrile (30 g, 152.3 mmole), potassium acetate (222.4 g, 228.5 mmole), and 18-crown-6 ether (60.4 g, 288.5 mmole) in MeCN (400 mL) was heated at reflux in 36 h. The mixture was cooled, added 2.5 N NaOH (200 mL), stirred at RT overnight. The mixture was extracted with ether (discarded). The aqueous layer was acidified with 6N HCl, extracted with EtOAc, dried over MgSO4, concentrated, purified by flash column chromatography (40% EtOAc/Hex) to give a light yellow foam (24.45 g, 81%). 1H-NMR (300 MHz, DMSO-d6): δ7.13 (dd, J=1.7, 8.3 Hz, 1H), 7.17 (d, J=1.7 Hz, 1H), 7.61 (d, J=8.3 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417215B1
Source datasetuspto-grants-2002_07
ORD IDord-3b86e109a0a547669f6f7bae59c0e693
Source noteuspto-grants-2002_07