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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814642Generated: October 25, 2026

n-Butyl lithium → 8-Cyclopropylidene-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/reaction/1814642

Reaction equation

Participants

RoleNameHCIDCharge
Reactantn-Butyl lithiumHCID 61028—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantCyclopropyltriphenylphosphonium bromideHCID 2723931—
SolventTetrahydrofuranHCID 8028—
Product8-Cyclopropylidene-1,4-dioxaspiro[4.5]decaneHCID 2250224953.3%

Reaction Conditions

Temperature-60 °C

Reaction Steps

Cyclopropyltriphenylphosphonium bromide (10.8 g, 28 mmol) was suspended in dry THF (30 mL) and cooled to −60° C. N-Butyllithium (1.6M in THF, 17 mL, 27 mmol) was added dropwise at −40 to −60° C. The temperature was raised to 20° C. and after 3 hours at this temperature, the reaction mixture was cooled to −60° C. 1,4-Cyclohexane dione mono ethylene ketal (4.0 g, 26 mmol) dissolved in THF (30 mL) was added at −60° C. whereafter the temperature was raised to 20° C. After 16 hours the reaction mixture was diluted with THF (75 mL) filtered through hyflo and concentrated in vacuo. The residue was purified by flash chromatography (4×15 cm column of silica) using heptane and ethyl acetate (4:1) as eluent to give 2.5 g of 8-cyclopropylidene-1,4-dioxa-spiro[4.5]decane (cf Synthetic Communications 21(20), 2015-2023, 1991).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875760B2
Source datasetuspto-grants-2005_04
ORD IDord-ab448ecb98d64a12b803e5c3defced3e
Source noteuspto-grants-2005_04