HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249332Generated: November 1, 2026
Cycloheptanol, 2,2,7,7-tetramethyl-1-(2-propenyl)- → HCID 13782557, compound
https://huagongshe.com/reaction/1249332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cycloheptanol, 2,2,7,7-tetramethyl-1-(2-propenyl)- | HCID 184493 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 13782557 | HCID 13782557 | 77.6% |
Reaction Steps
1-Allyl-2,2,7,7-tetramethylcycloheptan-1-ol (15.00 g, 0.09 moles), 5 wt % Pd/C (1.00g, 0.33 wt % Pd) and n-hexane (20 ml) were added to an autoclave. The air in the autoclave was replaced by nitrogen, followed by applying to a H2 pressure of 50 atm and heating the autoclave to 50° C. under stirring. The reaction was determined as completed at the time when the gas absorption was stopped. It required about 2 hours in this case. The autoclave was cooled down to room temperature and returned to a normal pressure, after which the content was withdrawn. The content was concentrated and subjected to fractionation to obtain 11.90 g (yield 77.6%) of the captioned compound. This compound was a colorless transparent liquid having a woody, earthy and patchuli oil-like odor.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04631147 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-74c9e1e5c3bc4558809f7177cd877db9 |
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| Source note | uspto-grants-1986_12 |
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