HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457232Generated: October 31, 2026
Water → 3,4,5,6-Tetrakis[(naphthalen-2-yl)oxy]benzene-1,2-dicarbonitrile
https://huagongshe.com/reaction/1457232
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86753409 | HCID 86753409 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,4,5,6-Tetrakis[(naphthalen-2-yl)oxy]benzene-1,2-dicarbonitrile | HCID 22104057 | — |
Reaction Steps
Preparation of 1,2-dicyano-3,4,5,6-tetra(2-naphthoxy)benzene 1,2-Dicyano-3,4,5,6-tetrachlorobenzene (30.5 parts), potassium carbonate (62.8 parts) and 2-naphthol (98.1 parts) were stirred in dimethylformamide (140 parts) at 70° C. for 3 hours. The mixture was poured into water (300 parts) and extracted with chloroform (3×300 parts). The combined chloroform extracts were washed with dilute aqueous sodium hydroxide solution (500 parts) and then with water (500 parts). The chloroform was dried over anhydrous magnesium sulphate before evaporating under reduced pressure to leave a brown liquid which crystallised on adding butan-1-ol, cooling and standing for 2 hours. The crystallised solid was filtered, washed with butan-1-ol until the filtrates were colourless. The solid was dried to give 1,2-dicyano-3,4,5,6-tetra(2-naphthoxy)benzene (40.6 parts), m.p. 188°-190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05847114 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-1b0abd7aba734dbe832a9f2b78d5424e |
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| Source note | uspto-grants-1998_12 |
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