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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633411Generated: November 1, 2026

Methyl iodide → 2,4-Dimethylspiro[5.5]undeca-1,4,8-trien-3-one

https://huagongshe.com/reaction/1633411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,3-ButadieneHCID 7845—
ReactantPhenol, 4-[(dimethylamino)methyl]-2,6-dimethyl-HCID 39355—
SolventEthyl AcetateHCID 8857—
Product2,4-Dimethylspiro[5.5]undeca-1,4,8-trien-3-oneHCID 1353145587.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a 250 mL glass reaction vessel containing an ethyl acetate (120 mLs) solution of N,N-dimethyl,2,6-dimethyl-4-aminomethylphenol (3.58 g; 20 mmols), there was added methyl iodide (20 mmols) to give a colorless slurry. The reaction vessel was sealed and 1,3-butadiene (100 mmols) was introduced into the system. The reaction mixture was heated to 120° C. and the pressure was increased from atmospheric up to 70 psig. The reaction mixture was maintained at these conditions for approximately 16 hours. The reaction vessel was then cooled to room temperature. After cooling, the reaction mixture was filtered to remove ammonium iodide salt by-product. The filtrate was concentrated to afford a viscous oil which was crystallized from ethanol to give 3.3 g of 2,4-dimethylspiro[5.5]undeca-1,4,8-trien-3-one (84% yield by vapor phase chromatography).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04480133
Source datasetuspto-grants-1984_10
ORD IDord-0a1ddec862814f128d3b64edba878b33
Source noteuspto-grants-1984_10