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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278621Generated: October 27, 2026

4-(4-Diisopropylaminomethylbenzoyl)-1-tritylpiperidine → 4-(4-Diisopropylaminomethylbenzoyl)piperidine

https://huagongshe.com/reaction/278621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Diisopropylaminomethylbenzoyl)-1-tritylpiperidineHCID 22627953—
SolventAcetic AcidHCID 176—
Product4-(4-Diisopropylaminomethylbenzoyl)piperidineHCID 22628177138.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-(4-diisopropylaminomethylbenzoyl)-1-tritylpiperidine (1.3 g) and 80% acetic acid aqueous solution (20 ml) was stirred at 80° C. for 1 hour and concentrated. To the residue was added water, and the solution was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and concentrated to give an oil of 4-(4-diisopropylaminomethylbenzoyl)piperidine (1.0 g). To a solution of the oil (302 mg) in THF (10 ml) was added 6-chloronaphthalene-2-sulfonylchloride (261 mg), and the mixture was stirred at room temperature for 1 hour. To the mixture was added sodium hydrogen carbonate aqueous solution, and the mixture was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography and eluted with hexane-ethyl acetate (4:1) to give the title compound (0.15g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359134B1
Source datasetuspto-grants-2002_03
ORD IDord-131a4c63a0dc4ee9ae01e5dc1722fb06
Source noteuspto-grants-2002_03