HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978993Generated: October 29, 2026
Trimethylsilyl iodide → HCID 178450321, compound
https://huagongshe.com/reaction/978993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | HCID 178450320 | HCID 178450320 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178450321 | HCID 178450321 | 84.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04666510 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-b2dc83bd724d4414890463d27c224ea4 |
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| Source note | uspto-grants-1987_05 |
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