HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030689Generated: October 26, 2026
1-Chloro-3-methyl-2-butene → Ethanone, 1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-
https://huagongshe.com/reaction/1030689
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloro-3-methyl-2-butene | HCID 10429 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2',4',6'-Trihydroxyacetophenone | HCID 68073 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethanone, 1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]- | HCID 11687311 | 55% |
Reaction Steps
In 250 ml of anhydrous tetrahydrofuran was dissolved 50.0 g of 2',4',6'-trihydroxyacetophenone, and 123.15 g of anhydrous potassium carbonate was added to the solution and the mixture was stirred at room temperature for 30 minutes. Then, 37.23 g of 1-chloro-3-methyl-2-butene was dropped into the solution over a period of 20 minutes and a reaction was carried out at room temperature for 24 hours. After the reaction, the reaction mixture was extracted with 2 l of ethyl acetate, and the ethyl acetate layer was washed with water (500 ml×4 times), shaken with a saturated aqueous solution of sodium chloride (300 ml×2 times), dried with anhydrous sodium sulfate and filtered. The solvent was removed from the filtrate by distillation and the obtained residue was recrystallized from a mixed solvent of benzene and petroleum ether to obtain 38.6 g (yield=55.0%) of 2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone in the form of a yellow prism.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05106871 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-a004afdfb9e44566a944b50ca94dcd1a |
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| Source note | uspto-grants-1992_04 |
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