HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127728Generated: October 25, 2026
4-Benzhydrylpiperidine → HCID 12796197, compound
https://huagongshe.com/reaction/127728
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Benzhydrylpiperidine | HCID 88278 | — |
| Reactant | HCID 12796194 | HCID 12796194 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 12796197 | HCID 12796197 | 149.6% |
Reaction Steps
To a solution of 9.75 grams (26.39 millimoles) of 6-(3,5-dioxomorpholino)hexyl p-toluenesulfonate (prepared as described in Example IX) in 160 milliliters of warm tertiary butyl alcohol was added portionwise at temperatures in the range of 30°-32° C. over a period of about 23 minutes, 63 grams (26.38 millimoles) of 4-benzhydrylpiperidine in 160 milliliters of tertiary-butyl alcohol. The reaction mixture was heated at reflux temperature for about 22 hours and thereafter the solvent removed by vaporization to obtain 17.7 grams of a 4-[6-(4-benzhydrylpiperidino)hexyl]-3,5-dioxomorpholine product as a yellow oil. Crystallization (twice) from ethyl acetate produced 4.19 grams of white crystals, m.p., 121°-124.5° C. and having NMR, UV and IR spectral characteristics appropriate for the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04256891 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-555f25c28eb04998b04b819d870496e5 |
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| Source note | uspto-grants-1981_03 |
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