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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978993Generated: October 29, 2026

Trimethylsilyl iodide → HCID 178450321, compound

https://huagongshe.com/reaction/978993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 178450320HCID 178450320—
SolventAcetonitrileHCID 6342—
ProductHCID 178450321HCID 17845032184.7%

Reaction Steps

Iodotrimethylsilane (0.5 ml) was added to a solution of 2-butyryl-3-hydroxy-5-(3-methoxymethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (1.50 g; 4.36 mmole) (see Example 36) in dry acetonitrile (10 ml) under nitrogen and the mixture was stirred at room temperature for 15 minutes. The solvent was evaporated and the residue was stirred with an ethanolic potassium hydroxide solution at room temperature for 15 hours. The solution was poured into dilute hydrochloric acid and then extracted with diethyl ether. The ether extract was dried over anhydrous magnesium sulfate and evaporated under reduced pressure. Purification by column chromatography over silica gel (eluant dichloromethane) gave 2-butyryl-5-(3-ethoxymethyl-2,4,6-trimethylphenyl)-3-hydroxycyclohex-2-en-1-one (1.32 g; 84.7%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04666510
Source datasetuspto-grants-1987_05
ORD IDord-b2dc83bd724d4414890463d27c224ea4
Source noteuspto-grants-1987_05