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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231215Generated: November 1, 2026

4-Bromopyridine → 8-(4-Pyridinyl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/231215

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromopyridineHCID 14268—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product8-(4-Pyridinyl)-1,4-dioxaspiro[4.5]decan-8-olHCID 1377205367.2%

Reaction Steps

Thirty-five ml of ether was cooled to -78° C., to which 20 ml of a 1.6 mol n-butyl lithium solution in hexane was added. Next, 5 g of 4-bromopyridine was dissolved in 30 ml of ether and the solution was added to the mixture. Then, a solution of 5 g of 1,4-cyclohexanedione monoethyleneacetal in 30 ml of tetrahydrofuran was added to the mixture. After completion of the reaction, the reaction solution was poured into saturated ammonium chloride aqueous solution. The mixture was extracted with chloroform and the extract was purified to give 5 g of 4-hydroxy-4-(4-pyridyl)cyclohexanone ethyleneacetal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845228
Source datasetuspto-grants-1989_07
ORD IDord-424fabbef7374f15a0447ba7747e7663
Source noteuspto-grants-1989_07