HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25911Generated: October 29, 2026
Methanol → 4H-Pyran-4-one, 2-Et-3-hydroxy-6-Me-
https://huagongshe.com/reaction/25911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | 1-(5-Methylfuran-2-yl)propan-2-ol | HCID 20468602 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4H-Pyran-4-one, 2-Et-3-hydroxy-6-Me- | HCID 10530228 | 30% |
Reaction Steps
In a three necked round bottom flask were combined 28 ml of methanol and 38 ml of water. The solution was cooled to -15° C. and 0.166 mole of 5-methyl-2-(2-hydroxy-propyl)furan (J. Org. Chem., 26, 1673, 1960) and 0.416 mole of chlorine were added simultaneously. During the addition, the reaction was maintained between -16° and -8° C. When addition was completed, the solution was warmed to 80° C. and refluxed for about 3 hours. Upon cooling to room temperature, the pH was adjusted to 2.1 and extracted with chloroform (3×100 ml). The combined organic layers were washed with water, brine and dried over magnesium sulfate. The organic solution was filtered and evaporated to give a thick dark solid. The solid was recrystallized twice from methanol to give 8.06 grams (30% yield) of white solid. Sublimation yielded pure product, m.p. 157°-159° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04147705 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-9017833b0ee54ebc83dd2420b77e13a5 |
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| Source note | uspto-grants-1979_04 |
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