HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352436Generated: October 30, 2026
Hydrochloric Acid → HCID 22712056, compound
https://huagongshe.com/reaction/352436
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | 3-((2-Hydroxyethyl)amino)propanol | HCID 3015059 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22712056 | HCID 22712056 | 15.6% |
Reaction Steps
6 g of 2-hydroxyethyl-3-hydroxypropylamine and 18,9 g of 1-benzyl-4-piperidone are taken up in 250 ml of methylene chloride and combined at 0° C. with 21.2 g of sodium triacetoxyborohydride. The mixture is stirred over night at ambient temperature, then acidified with 2 N hydrochloric acid and made alkaline with concentrated sodium hydroxide solution. It is extracted with methylene chloride, the extract is dried over sodium sulphate and the solvent is eliminated in vacuo. The residue is chromatographed with ethyl acetate/methanol/conc. ammonia solution 20:80:1 over silica gel. The fractions found to be uniform by TLC are combined and the solvent is eliminated in vacuo. 2.3 g of 1-benzyl-4-[(2-hydroxy-ethyl)-(3-hydroxy-propyl)-amino]-piperidine are obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747044B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-4c6545431c7945f394a4c3ba1250275e |
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| Source note | uspto-grants-2004_06 |
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