HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648355Generated: October 29, 2026
Sodium Iodide → 1-[3-(Diphenylamino)propyl]-4-(3-fluorophenyl)-4-piperidinol ethanedioate
https://huagongshe.com/reaction/648355
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-[N,N-diphenylamino)-1-bromopropane | HCID 10827329 | — |
| Reactant | 4-(3-Fluorophenyl)piperidin-4-ol | HCID 12763906 | — |
| Product | 1-[3-(Diphenylamino)propyl]-4-(3-fluorophenyl)-4-piperidinol ethanedioate | HCID 86738023 | — |
Reaction Steps
A mixture of 10.4 g (0.018 moles) of 3-[N,N-diphenylamino]-1-bromopropane, 3.5 g. (0.018 moles) of 4-(3-fluorophenyl)-4-piperidinol, 1.9 g. (0.018 moles) of sodium carbonate and 1.0 g. of sodium iodide in 100 ml. of methyl ethyl ketone is refluxed for about 3 hours. The reaction is allowed to cool, filtered and the filtrate is evaporated. The residue is shaken with a mixture of diethyl ether and dilute hydrochloric acid. An oily third phase forms which crystallizes on scratching. This material is recrystallized from isopropanol and then from ethanol, and converted back to the free base. The product is then crystallized from isopropanol containing an excess of oxalic acid giving 2.2 g. of 1-[3-(diphenylamino)propyl]-4-(3-fluorophenyl)-4-piperidinol ethanedioate (1:1), mp. 181°-182.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04411904 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-4fd70594539940c88e39080309ecc674 |
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| Source note | uspto-grants-1983_10 |
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