HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38391Generated: October 30, 2026
Water → 2-(1-Hydroxy-1-methyl-ethyl)-3-methoxy-phenol
https://huagongshe.com/reaction/38391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(2-Hydroxy-6-methoxyphenyl)ethan-1-one | HCID 69709 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-Hydroxy-1-methyl-ethyl)-3-methoxy-phenol | HCID 59598645 | — |
Reaction Steps
To a solution of methyl magnesium bromide (24 mL of a 3M solution in diethyl ether, 72.2 mmol) in anhydrous tetrahydrofuran (20 mL) at 0° C. was added a solution of 2′-hydroxy-6′-methoxyacetophenone (4 g, 24.1 mmol) in anhydrous tetrahydrofuran (40 mL), maintaining the temperature below 11° C. during the addition. After stirring for 1.5 hours at room temperature, a solution of 10% ammonium chloride (30 mL) was added slowly maintaining the temperature below 22° C. with the use of an ice bath. Water (300 mL) was slowly added and the reaction was extracted twice with ethyl acetate. The combined ethyl acetate layers were washed with water, brine, dried using anhydrous sodium sulfate and concentrated to give 2-(1-Hydroxy-1-methyl-ethyl)-3-methoxy-phenol (4.52 g) as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524725B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-49811de14cd74c70be85a142c4a145ad |
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| Source note | uspto-grants-2013_09 |
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