HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721852Generated: October 31, 2026
p-Fluoronitrobenzene → HCID 14649986, compound
https://huagongshe.com/reaction/1721852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 11715514 | HCID 11715514 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14649986 | HCID 14649986 | 77.29% |
Reaction Steps
A stirred suspension of sodium hydride (60% in oil, 1.00 g) in 50 ml of dimethylformamide was treated with a solution of 4.0 g of 1-acetyl-4-hydroxy-4-phenylpiperidine in 100 ml of dimethylformamide. The mixture was heated at 70° C. until evolution of gas had ceased. After cooled to ice bath temperature, a solution of 2.96 g of 1-fluoro-4-nitrobenzene in 40 ml of dimethylformamide was added, dropwise, and the reaction allowed to proceed for 20 hours. The reaction mixture was then poured into ice water and the aqueous suspension extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated to an oil. High pressure liquid chromatography of the oil (silica gel; elution with 20% ethyl acetate/dichloromethane) afforded 4.73 g (77.29%) of 1-acetyl-4-(4-nitrophenoxy)-4-phenylpiperidine, m.p. 145°-150° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04853384 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-f3f423d25f6e4f0190d14f463c0ab7a5 |
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| Source note | uspto-grants-1989_08 |
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