Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735292Generated: November 1, 2026

1,4-Dioxaspiro[4.5]decan-8-one → 8-(2-Chlorophenylmethylene)-1,4-dioxaspiro[4.5]decane

https://huagongshe.com/reaction/1735292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
Reactant2-Chlorophenylmethyltriphenylphosphonium bromideHCID 16731598—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product8-(2-Chlorophenylmethylene)-1,4-dioxaspiro[4.5]decaneHCID 1970520481.4%

Reaction Steps

A stirred solution of 18.0 grams (0.039 mole) of 2-chlorophenylmethyltriphenylphosphonium bromide in about 50 mL of dry tetrahydrofuran was cooled in a dry ice-acetone bath, and 15.4 mL (0.039 mole) of n-butyllithium (2.5M in hexanes) was added dropwise. Upon completion of addition, the reaction mixture was stirred for 1 hour. After this time a solution of 5.0 grams (0.032 mole) of 1,4-cyclohexanedione mono-ethylene ketal in about 5.0 mL of dry tetrahydrofuran was added dropwise. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature where it was stirred for about 18 hours. After this time the reaction mixture was concentrated under reduced pressure, yielding about 6.9 grams of 8-(2-chlorophenylmethylene)-1,4-dioxaspiro[4.5]-decane. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536725
Source datasetuspto-grants-1996_07
ORD IDord-804072f9caaf4189af8ac23507d3a74a
Source noteuspto-grants-1996_07