HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397591Generated: October 29, 2026
Hydrochloric Acid → HCID 10127387, compound
https://huagongshe.com/reaction/397591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidine, 1-(2-chloroethyl)-, hydrochloride | HCID 74826 | — |
| Reactant | HCID 12114663 | HCID 12114663 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10127387 | HCID 10127387 | — |
Reaction Steps
A mixture of (4-methoxyphenyl)-(4-hydroxyphenyl)-1,2,3,4-tetrahydronaphth-1-yl-methane (400 mg 0.0011 mol), anhydrous K2CO3 (2.0 gm, 0.014 mol), 1-(2-chloroethyl)piperidine hydrochloride (400 mg, 0.002) and dry acetone (25.0 ml) was refluxed for 10 hrs, K2CO3 was filtered off acetone was distilled off and residue was diluted with water. The reaction mixture was extracted with ethyl acetate, washed with water, dried over sodium sulphate and concentrated to give an oil which was filtered through basic alumina column by using benzene as eluent, and was concentrated. The oil thus obtained was treated with ethanolic HCl. The solvent was evaporated and compound was crystallized with absolute alcohol and anhydrous ether, and filtered under anhydrous conditions to give title compound of formula I. Yield 310 mg. (58.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610705B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-09416c980e3941ba9f0ce52ae3e5d44d |
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| Source note | uspto-grants-2003_08 |
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