HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107864Generated: October 30, 2026
Hydrochloric Acid → 3-Methyl-6-hydroxybenzofuran
https://huagongshe.com/reaction/1107864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (3-Hydroxyphenoxy)acetone | HCID 18786125 | — |
| Product | 3-Methyl-6-hydroxybenzofuran | HCID 10855624 | 60.4% |
Reaction Steps
3 g (18 mmol) of (3-hydroxyphenoxy)acetone and 400 ml of a 0.1M potassium hydroxide solution are introduced into a 1 l three-necked flask equipped with a reflux condenser. Heating is carried out at reflux for 6 hours. The reaction mixture is cooled to 5° C., a molar hydrochloric acid solution is added, in order to obtain a pH of approximately 5, and extraction is carried out with ethyl ether (3×150 ml). The organic phases are combined, dried over magnesium sulphate and concentrated. The residue is purified by silica column chromatography (elution solvent: 8/2 cyclohexane/ethyl acetate). 1.61 g of 3-methyl-6-hydroxybenzofuran are obtained--M.p.: 92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06063810 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-80cae4e0f7424c6ea2f4512a170fc7a7 |
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| Source note | uspto-grants-2000_05 |
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