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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015997Generated: October 30, 2026

1,4-Dioxaspiro[4.5]decan-8-one → 8-[6-(1-Azetidinyl)-3-pyridinyl]-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/1015997

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
Reactant2-(Azetidin-1-yl)-5-bromopyridineHCID 18329833—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product8-[6-(1-Azetidinyl)-3-pyridinyl]-1,4-dioxaspiro[4.5]decan-8-olHCID 5955610543%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-azetidin-1-yl-5-bromopyridine (64 mg, 0.30 mmol) was dissolved in dry THF (1.5 mL) and cooled to −78° C., followed by the addition of n-BuLi (0.196 mL, 1.6 M in hexanes). Thirty minutes later, a solution of 1,4-cyclohexanedione mono-ethylene ketal (44.6 mg, 0.286 mmol) in dry THF (0.2 mL) was added dropwise at −78° C. with constant stirring. One hour later, the reaction was quenched with NH4Cl (aq) and slowly warmed to rt. The aqueous layer was extracted with CH2Cl2×3, dried, filtered and concentrated to give a crude, which was purified by flash column chromatography (100% EtOAc) to provide 35 mg (43%) of white solid product. MS (M+H+)=291.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985730B2
Source datasetuspto-grants-2011_07
ORD IDord-b7090672bd724e39a3dc719d4f14a7ad
Source noteuspto-grants-2011_07