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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434698Generated: October 30, 2026

Piperidine → 10-(1-Piperidinyl)-5H-dibenzo[a,d]cyclohepten-5-one

https://huagongshe.com/reaction/434698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant10-Bromo-5H-dibenzo[a,d][7]annulen-5-oneHCID 12437215—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product10-(1-Piperidinyl)-5H-dibenzo[a,d]cyclohepten-5-oneHCID 11098226—

Reaction Steps

A mixture of 71.3 g of 10-bromo-5H-dibenzo[a,d]cyclohepten-5-one, 50 ml. of piperidine, 1 liter of t-butanol and finally 33.6 g of potassium t-butoxide was stirred under reflux 2 hours, then at room temperature overnight. The mixture was filtered, and concentrated to dryness. The residue was slurried with water and decanted. The residue was slurried with methanol and filtered to give 59.8 g of 10-(1-piperidyl)-5H-dibenzo[a,d]cyclohepten-5-one, m.p. 103°-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04399141
Source datasetuspto-grants-1983_08
ORD IDord-0f26040b80254976847da16edf57f8f8
Source noteuspto-grants-1983_08