HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216029Generated: October 29, 2026
1,4-Dioxane → 4-allyl-N-(3-chlorophenyl)piperidine-4-carboxamide
https://huagongshe.com/reaction/216029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Tert-butyl 4-allyl-4-(3-chlorophenylcarbamoyl)piperidine-1-carboxylate | HCID 67036827 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-allyl-N-(3-chlorophenyl)piperidine-4-carboxamide | HCID 68991112 | — |
Reaction Steps
To a solution of tert-butyl 4-allyl-4-(3-chlorophenylcarbamoyl)piperidine-1-carboxylate from step A (0.172 g, 0.453 mmol) in MeOH (10 mL) was added 4 MHCl in dioxane (0.340 mL, 1.36 mmol). The reaction was heated at 50° C. for 30 min, and then concentrated under vacuum, re-dissolved in MeOH and re-concentrated twice to give the title compound as the hydrochloride salt. MS (ES+) [M+H]+=279.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193202B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-6498dcf92aa943d1b591ff9b658bcf7e |
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| Source note | uspto-grants-2012_06 |
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