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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273519Generated: November 1, 2026

Pyridinium hydrochloride → HCID 58050245, compound

https://huagongshe.com/reaction/2273519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium hydrochlorideHCID 21584435—
ReactantHCID 58050238HCID 58050238—
SolventWaterHCID 962—
ProductHCID 58050245HCID 5805024560.6%

Reaction Steps

9-(2,6-Dimethoxyphenyl)-9H-carbazole (10.00 g) and pyridinium hydrochloride (50.0 g) were placed in the 250 ml round-bottom flask, equipped with magnetic stirrer and immersed in the pre-heated oil bath (230° C., 45 min). The reaction mixture was cooled down to room temperature, diluted with 400 ml water and extracted with ethyl acetate (3×150 ml). Organic fractions were combined, dried over sodium sulfate anhydrous, filtered and evaporated, providing 5.5 g of pure 2-carbazol-9-yl-benzene-1,3-diol. 2-Carbazol-9-yl-benzene-1,3-diol (5.5 g, 20 mmol) and pyridine (6.0 ml) were dissolved in 50 ml DCM (anhydrous) and cooled in the ice bath. Solution of triflic anhydride (6.0 ml) in 20 ml DCM was added dropwise upon intensive stirring, reaction mixture was warmed up to room temperature and stirred overnight. The reaction mixture was washed with water, dried over sodium sulfate, filtered and evaporated, providing crude triflate. Pure material (white solid, 6.0 g) was obtained by column chromatography on silica gel (eluent hexane/ethyl acetate 1/1 mixture).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09123903B2
Source datasetuspto-grants-2015_09
ORD IDord-80f4fc4cab4e47e6967dffb12a0729b9
Source noteuspto-grants-2015_09