HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985750Generated: October 30, 2026
HCID 70053, compound → HCID 178516049, compound
https://huagongshe.com/reaction/985750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 70053 | HCID 70053 | — |
| Reactant | HCID 11184696 | HCID 11184696 | — |
| Product | HCID 178516049 | HCID 178516049 | — |
| Product | HCID 178516050 | HCID 178516050 | — |
Reaction Steps
More particularly, 1,4-bis(4-hydroxyphenyl)-1-cyclohexene is hydrogenated, and the resulting reaction mixture which contains 4-(4′-(4″-hydroxyphenyl)cyclohexyl)-1-hydroxybenzene is subjected to conventional purification methods to provide a purified product, and the product is then dissolved in an organic solvent which is suitably used in column separation processes, such as methanol, acetonitrile or tetrahydrofuran, or alternatively, the reaction mixture obtained is subjected to solvent replacement by an organic solvent which is suitably used in column separation processes, such as methanol, acetonitrile or tetrahydrofuran. Then, the resulting solution of the product or the solution of the reaction mixture in such an organic solvent as mentioned above is subjected to cis-trans separation operations by a suitable means such as preparative high performance liquid chromatography making use of difference of retention time so that the cis- and trans-isomer, that is, 4-(trans-4′-(4″-hydroxyphenyl)cyclohexyl)-1-hydroxybenzene and 4-(cis-4′-(4″-hydroxyphenyl)cyclohexyl) 1-hydroxybenzene, are separately obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06872858B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-5dd69dcf06ff40a6a71231b07b4376c5 |
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| Source note | uspto-grants-2005_03 |
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