HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030684Generated: October 26, 2026
Tetrahydrofuran → 2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(2-propenyl)acetophenone
https://huagongshe.com/reaction/1030684
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethyl Ether | HCID 8254 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2',4',6'-Trihydroxy3'-(2-propenyl)acetophenone | HCID 14368078 | — |
| Product | 2'-Hydroxy-4',6'-bis(methoxymethoxy)-3'-(2-propenyl)acetophenone | HCID 19744885 | 94.7% |
Reaction Steps
In 160 ml of anhydrous tetrahydrofuran were dissolved 18.4 g of the so-obtained 2',4',6'-trihydroxy3'-(2-propenyl)acetophenone and 57.1 g of N,N-diisopropylethylamine, and 28.4 g of chrolomethyl methyl ether was added to the solution under ice cooling and the reaction mixture was stirred under ice cooling for 1 hour, and further, stirred at room temperature for 4 hours to effect a reaction. The reaction mixture was extracted with diethyl ether and filtered, and the solvent was removed from the filtrate by distillation. The obtained residue was subjected to the silica gel column chromatography [eluting solvent=n-hexane/ethyl acetate (7/1)] to obtain 24.8 g (yield=94.7%) of 2'-hydroxy-4',6'-bismethoxymethoxy-3'-(2-propenyl)acetophenone in the form of a colorless oil.
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-7a22d84775e5409a8259bce92fa8e549 |
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| Source note | uspto-grants-1992_04 |
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