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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112758Generated: October 26, 2026

4-Benzhydrylpiperidine → HCID 12796197, compound

https://huagongshe.com/reaction/1112758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BenzhydrylpiperidineHCID 88278—
Reactant6-(3,5-Dioxomorpholino)hexyl p-toluenesulfonateHCID 12796194—
Solventtert-ButanolHCID 6386—
ProductHCID 12796197HCID 12796197149.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123538
Source datasetuspto-grants-1978_10
ORD IDord-d49c926f5ed24032a915bb655bc778d4
Source noteuspto-grants-1978_10