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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515901Generated: October 30, 2026

4-Aminophenol → HCID 131733314, compound

https://huagongshe.com/reaction/515901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant6-Chloropyridine-2-carbonitrileHCID 118424—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 131733314HCID 131733314—

Reaction Conditions

Temperature145 °C

Reaction Steps

4-Aminophenol (3.3 g, 30.2 mmol) is added to a solution of 6-chloropyridine-2-carbonitrile (3.5 g, 25.3 mmol) in 1-methyl-2-pyrrolidinone (70 mL). The reaction mixture is heated at 140-150° C. for 16 hours in a sealed flask. The batch is then cooled to ambient temperature. Imidazole (3.4 g, 49.9 mmol) and tert-butyl(dimethyl)silyl chloride (7.6 g, 50.4 mmol) are subsequently added and the mixture is stirred for 16 hours at ambient temperature. The mixture is diluted with water (140 mL) and the product is extracted with AcOEt (4×50 mL). The organic phases are combined and washed with water (3×50 mL), and then brine (1×50 mL). The organic phase is then dried over MgSO4, filtered and concentrated in vacuo. The crude product is purified by chromatography over silica gel using ethyl acetate and heptane as eluants to obtain the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-4f7fc03deec84e33aef3cbb33598a0b3
Source noteuspto-grants-2015_08