HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222858Generated: November 3, 2026
Cyclohexanol → 1-(Cyclohexyloxy)-4-nitrobenzene
https://huagongshe.com/reaction/222858
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(Cyclohexyloxy)-4-nitrobenzene | HCID 11962050 | — |
Reaction Steps
To 3.9 g of cyclohexanol (1.1 equivalents) put into the presence of 2.12 g of sodium hydride (1.5 equivalents) under stirring for 10 min, is added a solution of 5 g of 4-fluoronitrobenzene in 75 mL of dimethylformamide. The whole is heated to 60° C. for 5 hrs. After returning to room temperature, the medium is hydrolyzed and the reaction crude product is extracted with ethyl acetate several times. The organic phases are dried on magnesium sulfate, filtered and evaporated under reduced pressure. With a silica gel chromatography of the residue (cyclohexane and then cyclohexane/ethyl acetate: 98/2 and 90/10) 6.06 g of the desired product are able to be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207373B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-aab12bc5d989400caad636e918ce3c71 |
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| Source note | uspto-grants-2012_06 |
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