HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112755Generated: October 26, 2026
p-Toluenesulfonic acid → 4-(6-Piperidinohexyl)3,5-dioxomorpholine
https://huagongshe.com/reaction/1112755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| 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
p-toluenesulfonate. 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 | US04123538 |
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| Source dataset | uspto-grants-1978_10 |
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| ORD ID | ord-97428bf44ab245f69f5f4d0668cf9c31 |
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| Source note | uspto-grants-1978_10 |
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