HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459148Generated: October 26, 2026
Lithium Hydroxide → 3-(4-Hydroxy-3-methoxyphenyl)-2-methoxypropanoic acid
https://huagongshe.com/reaction/459148
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 3-(4-Hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid methyl ester | HCID 58823008 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Hydroxy-3-methoxyphenyl)-2-methoxypropanoic acid | HCID 18443662 | 74% |
Reaction Steps
A 1N aqueous lithium hydroxide solution was added to a solution of 3-(4-hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid methyl ester (280 mg, 1.17 mmol) in THF at room temperature, and the reaction mixture stirred overnight. The aqueous phase was extracted with ethyl acetate (20 mL), acidified to pH 2, and extracted with ethyl acetate (3×15 mL). The later organic layers were combined and washed with water (15 mL) and brine (10 mL), dried (MgSO4), filtered, and concentrated under vacuum to produce 3-(4-hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid as an oil (183 mg, 74%). 1H-NMR (250.13 MHz, CDCl3): δ 6.83 (1H, d, J=7.8), 6.74 (1H, s), 6.72 (1H, d, J=7.8), 3.99 (1H dd, J=7.8, 4.0), 3.85 (s, 3H), 3.40 (s, 3H), 3.09 (1H, dd, J=14.2, 4.0), 2.91 (1H dd, J=14.2, 7.8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192982B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-2d4d67a8859f406389ddf0bfde39991c |
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| Source note | uspto-grants-2007_03 |
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