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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35779Generated: October 27, 2026

Trimethylsilyl iodide → HCID 178450319, compound

https://huagongshe.com/reaction/35779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 178450320HCID 178450320—
CatalystSilver NitrateHCID 24470—
SolventAcetonitrileHCID 6342—
ProductHCID 178450319HCID 17845031987.7%

Reaction Steps

Iodotrimethylsilane (0.3 ml) was added to a solution of 2-butyryl-3-hydroxy-5-(3-methoxymethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (0.5 g, 1.45 mmole) (see Example 36) in dry acetonitrile (10 ml) under nitrogen and the mixture was stirred at room temperature for 15 minutes. An aqueous solution of silver nitrate was added and the mixture was stirred for a further 4 hours. The solvent was evaporated and the residue was washed successively with dilute aqueous sodium hydroxide and acetic acid, then dissolved in ethyl acetate and dried over anhydrous sodium sulfate. Evaporation under reduced pressure yielded 2-butyryl-3-hydroxy-5-(3-hydroxymethyl-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (0.42 g; 87.0%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767879
Source datasetuspto-grants-1988_08
ORD IDord-a3782001c16943e0ad4169429c50de1b
Source noteuspto-grants-1988_08