HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585665Generated: October 30, 2026
(+/-)-Methyl {4-[2,4-bis(methoxymethoxy)phenyl]cyclohexylidene}acetate → HCID 178497879, compound
https://huagongshe.com/reaction/585665
Participants
| Role | Name | HCID | Charge |
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| Reactant | (+/-)-Methyl {4-[2,4-bis(methoxymethoxy)phenyl]cyclohexylidene}acetate | HCID 91541557 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178497879 | HCID 178497879 | 99.3% |
Reaction Steps
To a round bottomed flask equipped with magnetic stirrer was added (±)-methyl {4-[2,4-bis(methoxymethoxy)phenyl]cyclohexylidene}acetate (1.13 g, 3.23 mmol) and ethanol (50 ml). To the stirred solution was added palladium (catalytic amount, 10% on activated carbon) in one portion. The reaction vessel was evacuated and placed under an atmosphere of hydrogen. This process was repeated for 10 cycles before leaving under a hydrogen atmosphere and then stirred vigorously for 17 hr. The reaction mixture was filtered through celite, washing with ethanol and the filtrate was evaporated to dryness, furnishing the title compound (1.13 g, 99%) as a colourless oil and a mixture of diastereoisomers. δH(CD3OD) 1.53 (2H, m), 1.62-1.78 (2H, m), 1.87 (4H, m), 2.93 (1H, m), 3.47 (3H, s), 3.51 (3H, s), 3.71 and 3.72 (3H, s), 5.16 and 5.17 (2H, s), 5.22 and 5.23 (2H, s), 6.66 and 6.68 (1H, d), 6.79 and 6.80 (1H, s), 7.12 and 7.15 (1H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933319B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-dd40ee033f7b4a1c916f33dcdb0d0d6b |
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| Source note | uspto-grants-2005_08 |
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