HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703622Generated: October 30, 2026
Acetic Acid → 4-(2,4-Dihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-one
https://huagongshe.com/reaction/703622
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-[4-(t-Butyldimethylsilyl)oxy-1,2-epoxy-2,6,6-trimethylcyclohexyl]but-3-en-2-one | HCID 54389374 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(2,4-Dihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-one | HCID 57090228 | 60.1% |
Reaction Steps
To 50 ml of a glacial acetic acid solution containing 600 mg of 4-[4-(t-butyldimethylsilyl)oxy-1,2-epoxy-2,6,6-trimethylcyclohexyl]but-3-en-2-one was added 8.9 g of a zinc powder at room temperature, and the mixture was vigorously stirred for 5 hours while maintaining the reaction temperature at about 40° C. To the reaction mixture was added 120 ml of chloroform, followed by stirring vigorously. Any insoluble matter was separated by filtration, and the filtrate was washed successively with water, a 5% aqueous solution of sodium hydrogen carbonate and water. The organic layer was dried over anhydrous magnesium sulfate, and the solvent, etc. were removed by distillation under reduced pressure. Purification of the resiude by silica gel chromatography gave 241 mg (yield: 55%) of 4-(2,4-dihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983723 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-aa2c4fb4eb26436f8ac9321b9ff4fcde |
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| Source note | uspto-grants-1991_01 |
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