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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659963Generated: October 31, 2026

Piperidine → 4-(6-Piperidinohexyl)3,5-dioxomorpholine

https://huagongshe.com/reaction/1659963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant6-(3,5-Dioxomorpholino)hexyl p-toluenesulfonateHCID 12796194—
Solventtert-ButanolHCID 6386—
Product4-(6-Piperidinohexyl)3,5-dioxomorpholineHCID 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 dichlormethanemethanol as eluant, (b) recovering from the effluent and (c) recrystallizing from tertiary butyl aclohol-ether, was a white solid, m.p. 121°-122.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04306063
Source datasetuspto-grants-1981_12
ORD IDord-d736808ef0e848178bd3378d20a7204a
Source noteuspto-grants-1981_12