HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395471Generated: October 26, 2026
Piperidine → 4-(6-Piperidinohexyl)3,5-dioxomorpholine
https://huagongshe.com/reaction/1395471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 6-(3,5-Dioxomorpholino)hexyl p-toluenesulfonate | HCID 12796194 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4-(6-Piperidinohexyl)3,5-dioxomorpholine | HCID 12796195 | — |
Reaction Steps
To a solution of 19.6 grams (53.2 millimoles) of 6-(3,5-dioxomorpholino)hexyl p-toluenesulfonate in 54 milliliters of tertiary butyl alcohol was added 5.3 milliliters of tertiary (53 millimoles) of piperidine in 54 milliliters of tertiary butyl alcohol. The reaction mixture was heated at reflux temperature for about 22 hours to obtain 4-(6-piperidinohexyl)-3,5-dioxomorpholine.p-toluenesulfonate product which crystallized from tertiary butyl alcohol-ether mixture in a yield of 13.45 grams (56 percent) as an off-white solid, m.p. 125°-128° C. A portion of this product after purification by (a) chromatographing on Silicar CC4 Special (Silica gel, product of Mallinkrodt) employing 10:1 dichloromethanemethanol as eluant, (b) recovering from the effluent and (c) recrystallizing from tertiary butyl alcohol-ether, was a white solid, m.p. 121°-122.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04203991 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-928b0a7152c54d7eab6689b028c95ffb |
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| Source note | uspto-grants-1980_05 |
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