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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280620Generated: October 25, 2026

Piperidine → 7-Bromo-2-(3-pyridylmethylene)-1-tetralone

https://huagongshe.com/reaction/280620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-PyridinecarboxaldehydeHCID 10371—
Reactant7-Bromo-1,2,3,4-tetrahydronaphthalen-1-oneHCID 252731—
SolventAcetic AcidHCID 176—
Product7-Bromo-2-(3-pyridylmethylene)-1-tetraloneHCID 5392235881.6%

Reaction Steps

A mixture of 7-bromo-1-tetralone (11.25 g), pyridin-3-carboxaldehyde (5.35 g), acetic acid (5 ml) and piperidine (6 ml) was heated on a steam bath for 6 hours and then allowed to stand for 18 hours. The volatile material was evaporated and the residue was dissolved in ethyl acetate. The solution was extracted several times with dilute hydrochloric acid and the combined extracts were made just alkaline with dilute sodium hydroxide solution. The solid was filtered off, washed with water and crystallised from methanol to give 7-bromo-2-(3-pyridylmethylene)-1-tetralone (12.8 g), m.p. 124°-125°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04590200
Source datasetuspto-grants-1986_05
ORD IDord-db01ba0aa6b644429b9baeab7006caf3
Source noteuspto-grants-1986_05