HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362771Generated: October 30, 2026
Hydrochloric Acid → HCID 131729849, compound
https://huagongshe.com/reaction/2362771
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 58000800 | HCID 58000800 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131729849 | HCID 131729849 | 83.2% |
Reaction Steps
To all ice cooled (0-5° C.) solution of aqueous concentrated HCl (7.0 mL, of 11 N, 77 mmol, 24 equiv.) in 95% ethanol (21 mL) was added dropwise a solution of 1,4-bis{3,4-bis[3-(piperidin-1-yl)propoxy]phenyl}-butane (2.50 g, 3.225 mmol) in 95% ethanol (21 mL)*. The solution was allowed to stir at 0-5° C. for three hours and the solvent was removed on a rotary evaporator keeping the temperature of the water bath at 45° C. The hydrochloride salt was dried under high vacuum for 48 hours. The crude product was then crystallized from ethanol:ether to give 2.46 g of the product (83.2% yield) after drying high vacuum for 72 hours. *Note that the starting material 1,4-bis{3,4-bis[3(piperidin-1-yl)propoxy]phenyl}-butane did not dissolve completely in 95% ethanol at room temperature, so the mixture was heated at 45° C. during which 1,4-bis{3,4-bis[3-(piperidin-1-yl)propoxy]phenyl}-butane dissolved. The solution was cooled to room temperature and added, to the ethanolic HCl solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691845B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-f28a225b78914b56aeaba5157010f998 |
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| Source note | uspto-grants-2014_04 |
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