HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850334Generated: November 1, 2026
Potassium Hydroxide → Ethyl (3,5-di-t-butyl-4-oxocyclohexa-2,5-dienylidene)acetate
https://huagongshe.com/reaction/850334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl (3,5-di-t-butyl-4-hydroxyphenyl)-acetate | HCID 13908126 | — |
| Catalyst | HCID 178511488 | HCID 178511488 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl (3,5-di-t-butyl-4-oxocyclohexa-2,5-dienylidene)acetate | HCID 22019852 | — |
Reaction Steps
In benzene (150 mL) was dissolved Intermediate 10 (6.7 g, 22.9 mmol) and this treated with a solution of potassium hydroxide (13.9 g [85%], 210 mmol) and potasium ferricyanide (K3Fe(CN)6) (15.2 g, 46 mmol) in water (150 mL). The mixture stirred under nitrogen atmosphere at 40° C. for 2 hours. The benzene layer then separated, washed with brine (100 mL) and dried over magnesium sulfate. The solvent was evaporated in vacuo to give a red oil, 6.1 g (92%), which was used as is.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017918 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-4eae0ab84fa34408a0f311abf2920d41 |
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| Source note | uspto-grants-2000_01 |
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