HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634596Generated: October 30, 2026
1,4-Dioxane → Ethyl 11-(p-hydroxyphenoxy)undecanoate
https://huagongshe.com/reaction/634596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Ethyl 11-(p-benzyloxyphenoxy)undecanoate | HCID 21259961 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 11-(p-hydroxyphenoxy)undecanoate | HCID 21260204 | 93.9% |
Reaction Steps
In a 1000 ml pressure resistant flask equipped with a stirrer were charged 100.0 g of ethyl 11-(p-benzyloxyphenoxy)undecanoate synthesized in Synthetic example 1, 3.0 g of a 10% palladium-carbon, 400 ml of 1,4-dioxane and 200 ml of ethanol, and the mixture was heated to 60° C. and under pressurized conditions of an inner vessel pressure at 2.5 kgf/cm2, a hydrogen gas was passed through and the mixture was vigorously stirred for 3 hours. Insolubles were removed by filtration, and the filtrate was concentrated to precipitate crystals. The resulting crystals were washed with cooled n-hexane to obtain 73.4 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06184180B2 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-3773137e695c4665af66681da06d780e |
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| Source note | uspto-grants-2001_02 |
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