HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587252Generated: October 25, 2026
Water → 3-(Hexyloxy)-6-hydroxybenzene-1,2-dicarbonitrile
https://huagongshe.com/reaction/1587252
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3-Dicyanohydroquinone | HCID 78467 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Hexyloxy)-6-hydroxybenzene-1,2-dicarbonitrile | HCID 15006689 | 31.8% |
Reaction Steps
27 g (168.8 mM) of 2,3-dicyanohydroquinone and 22.2 g (337 mM) of 85%-potassium hydroxide were dissolved in a mixture solvent of 65 ml of methanol and 302 ml of dimethylformamide, followed by heating to 50° C. To the solution, 33.4 g (202.4 mM) of hexyl bromide were added dropwise in 25 minutes, followed by heating to 100° C. and stirring for 3 hours. The reaction mixture was poured into cold water and washed with ether. The water layer was acidified with 6N-hydrochloric acid to provide a pH value of 1, followed by precipitation of a crystal. The crystal was extracted with ether, and the ether layer was washed with 5%-sodium hydrogen-carbonate aqueous solution and further washed with water, followed by distilling-off of the solvent to obtain a crude product. The crude product was treated with activated carbon and recrystalized from methanol to obtain 13.1 g of 2,3-dicyano-4-hexyloxyphenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05217643 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-1ef0cb99e25d4ae5bf721947c31adc49 |
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| Source note | uspto-grants-1993_06 |
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