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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(4-Diisopropylaminomethylbenzoyl)-1-tritylpiperidine | HCID 22627953 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(4-Diisopropylaminomethylbenzoyl)piperidine | HCID 22628177 | 138.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06359134B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-131a4c63a0dc4ee9ae01e5dc1722fb06 |
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| Source note | uspto-grants-2002_03 |
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