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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413257Generated: November 3, 2026

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

https://huagongshe.com/reaction/2413257

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 stream 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 numberUS04496572
Source datasetuspto-grants-1985_01
ORD IDord-46dea84cae274694b8b3834e7a6b459f
Source noteuspto-grants-1985_01