HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2407605Generated: November 1, 2026
4-tert-Butylcyclohexanone → HCID 10911276, compound
https://huagongshe.com/reaction/2407605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-tert-Butylcyclohexanone | HCID 7392 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Allyltrimethylsilane | HCID 69808 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10911276 | HCID 10911276 | 88% |
Reaction Steps
Into a two-necked flask were placed 4-tert-butylcyclohexanone (74.1 mg, 0.480 mmol), and toluene (5.0 ml) as a solvent, and the mixture was subjected to heating under reflux conditions under an argon atmosphere. After the start of the refluxing, allyltrimethylsilane (82.3 mg, 0.720 mmol) was added, and a solution (0.1 M) of triflic imide (1.35 mg, 4.80 μmol) in toluene was added dropwise. After 5 min, triethylamine (0.486 mg, 4.80 μmol) was added, and the mixture was reacted for 10 min. Thereafter, cooled aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with hexane and dried over sodium sulfate. The solvent was evaporated under reduced pressure and purified by column chromatography to give the object product 4-tert-butyl-1-trimethylsilyloxy-1-cyclohexene (yield 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809567B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-2daad67c6fdd4e6fb4e6e52045222baa |
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| Source note | uspto-grants-2014_08 |
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