HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965831Generated: November 1, 2026
HCID 67388428, compound → HCID 58444072, compound
https://huagongshe.com/reaction/1965831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67388428 | HCID 67388428 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58444072 | HCID 58444072 | 97.1% |
Reaction Steps
25.0 g of crude 4-(4-tert-butyl-phenyl)-2-(1-ethylcyclo-hexylmethylene)-indan-1-one (GC: ˜83% purity) are dissolved in 250 ml of ethyl acetate in a flask with gas inlet and stirrer. 1.75 g of palladium on activated carbon (10 wt-% palladium) are added. The system is evacuated and refilled with argon three times to remove oxygen and then evacuated and refilled with hydrogen three times. The stirrer is started and the reaction mixture is vigorously stirred to help the diffusion of hydrogen gas into the liquid reaction mixture. The hydrogen uptake is monitored and stirring is continued until the hydrogen uptake ceases. Filtering the crude reaction mixture over a paper filter and removing the solvent in a vacuum leaves crude 4-(4-tert-butyl-phenyl)-2-(1-ethyl-cyclohexylmethyl)-indan-1-one (yield 24.4 g, GC: ˜82% purity). The obtained crude product was used without further purification for the subsequent reduction/elimination-sequence.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415492B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-de3962b84f134e46aca96d0a52066ea9 |
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| Source note | uspto-grants-2013_04 |
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