HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676872Generated: October 31, 2026
Pyridinium hydrochloride → HCID 58050245, compound
https://huagongshe.com/reaction/1676872
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridinium hydrochloride | HCID 21584435 | — |
| Reactant | HCID 58050238 | HCID 58050238 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 58050245 | HCID 58050245 | 60.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08007927B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-87a1210cde9e40518c8200aad150b695 |
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| Source note | uspto-grants-2011_08 |
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