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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantPiperidineHCID 8082—
Reactant6-(3,5-Dioxomorpholino)hexyl p-toluenesulfonateHCID 12796194—
Solventtert-ButanolHCID 6386—
Product4-(6-Piperidinohexyl)3,5-dioxomorpholineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123538
Source datasetuspto-grants-1978_10
ORD IDord-97428bf44ab245f69f5f4d0668cf9c31
Source noteuspto-grants-1978_10