HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411998Generated: October 30, 2026
Benzyl Alcohol → Benzene, 1-nitro-4-(phenylmethoxy)-
https://huagongshe.com/reaction/411998
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Benzene, 1-nitro-4-(phenylmethoxy)- | HCID 70842 | 91.3% |
Reaction Steps
Benzyl alcohol (2.22 g, 20 mmol) was added to a slurry of hexane-washed NaH (60% oil suspension, 820 mg, 20.5 mmol) in DMSO (20 mL), stirred under nitrogen at 20° C., producing strong gas evolution. After 30 minutes, 1-fluoro-4-nitrobenzene (2.826 g, 20 mmol) was added dropwise to the light grey slurry. The reaction mixture became a bright orange red and quite strongly exothermic, and a lot of gas was evolved. After 2 hours, the reaction mixture was poured onto ice-water (200 mL), and the solid was collected by Buchner filtration, rinsed with water (2×50 mL), and air dried to give 1-benzyloxy-4-nitrobenzene (4.188 g, 91.3%) as canary yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562818B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-330a64cfd1f34451985b1efc040b0e5c |
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| Source note | uspto-grants-2003_05 |
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