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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421650Generated: November 2, 2026

Methyl iodide → 1,3-Cyclohexanedione, 2,5,5-trimethyl-

https://huagongshe.com/reaction/1421650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDimedoneHCID 31358—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product1,3-Cyclohexanedione, 2,5,5-trimethyl-HCID 136901—

Reaction Steps

28.0 g (0.2 mol) of dimedone were dissolved in 150 ml of absolute t-butanol and, at 40° C., 22.4 g (0.2 mol) of potassium t-butoxide were added a little at a time. After 2 hours, an equimolar amount of methyl iodide was added. After a further 2 hours, the solvent was removed under reduced pressure and the residue which remained was extracted 3 times with diethyl ether. The combined ether extracts were evaporated to dryness. Yield: 26.2 g (85%). The crude product was not purified further.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077965
Source datasetuspto-grants-2000_06
ORD IDord-32dc253c55404eaea20bbd9d01772a14
Source noteuspto-grants-2000_06