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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039420Generated: November 3, 2026

Pyridinium hydrochloride → HCID 58050245, compound

https://huagongshe.com/reaction/2039420

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 numberUS08580402B2
Source datasetuspto-grants-2013_11
ORD IDord-ccf038cb5f714e7392c828be109e1760
Source noteuspto-grants-2013_11