HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437561Generated: October 30, 2026
Benzene, 1-chloro-4-fluoro- → 1-Benzyl-4-(p-chlorophenoxy)piperidine
https://huagongshe.com/reaction/437561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene, 1-chloro-4-fluoro- | HCID 9604 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Benzylpiperidin-4-ol | HCID 78461 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyl-4-(p-chlorophenoxy)piperidine | HCID 21428714 | — |
Reaction Steps
A solution of 21.6 g of 1-benzyl-4-piperidinol in 75ml. of dimethylformamide is added slowly to a stirred suspension of 8.7 g of a 50% oil dispersion of sodium hydride in 225 ml. of dimethylformamide at 60°-70° C. After addition is complete stirring and heating are continued until no more hydrogen gas is liberated. A solution of 19.6 g of 1-chloro-4-fluorobenzene in 75 ml. of dimethylformamide is added, and the solution is permitted to stir at 65°-70° C. for 16 hours. After cooling to ambient temperature, the solution is poured into 600 ml. of water, the aqueous solution is extracted with benzene, the benzene extracts are dried, and the benzene is removed under reduced pressure, leaving a yellow oil of 1-benzyl-4-(p-chlorophenoxy)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04031221 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-fcf69e8b36014cb8b24ac1ad22295f2d |
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| Source note | uspto-grants-1977_06 |
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