HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950621Generated: October 29, 2026
Piperidine, 1-(2-chloroethyl)-, hydrochloride → HCID 11235858, compound
https://huagongshe.com/reaction/1950621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine, 1-(2-chloroethyl)-, hydrochloride | HCID 74826 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | HCID 11360078 | HCID 11360078 | — |
| Reactant | HCID 66628061 | HCID 66628061 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11235858 | HCID 11235858 | 34.4% |
Reaction Steps
Synthesized from 4-{5-methoxy-2-[2-(4-methoxyphenyl)ethyl]phenoxy}phenol and 1-(2-chloroethyl)piperidine hydrochloride according to an analogous synthetic method to Preparation Example 40, to 1-{2-{4-{5-methoxy-2-[2-(4-methoxyphenyl)ethyl]phenoxy}phenoxy}ethyl}piperidine (344 mg) was added pyridine hydrochloride (1.2 g), and the solution was stirred for 3 hours and 10 minutes at 170° C. To the reaction solution were added tetrahydrofuran and an aqueous solution of 1N sodium hydroxide, the solution was extracted with ethyl acetate, then washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (ethyl acetate-methanol system) to provide the title compound (111 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399520B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-b426420faa9e4c47b6d314080b1027ce |
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| Source note | uspto-grants-2013_03 |
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