HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007583Generated: October 25, 2026
Potassium Hydroxide → 3(S)-hydroxy-2-methylene-3-phenylpropanoic Acid
https://huagongshe.com/reaction/1007583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (+)Methyl 3(S)-hydroxy-2-methylene-3-phenylpropanoate | HCID 11008751 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3(S)-hydroxy-2-methylene-3-phenylpropanoic Acid | HCID 23520093 | — |
Reaction Steps
A solution of potassium hydroxide (2.27 g, 0.040 mol, 1.3 eq) in water (45 mL) was added drop wise to a solution of 1a (6 g, 0.031 mol, 1 eq) in methanol (15 mL) (see FIG. 4). The mixture was stirred at room temperature for 15 h. The solution was then concentrated under vacuum. The aqueous phase was washed with ether (2×100 mL), acidified with 6N aqueous HCl solution and extracted with ether (3×100 mL). The combined organic extracts were washed with brine (100 mL) and dried over sodium sulfate. Evaporation of the solvent afforded a colorless oil which crystallized upon standing. The desired product 9a was obtained as a solid (5.34 g, 96%). Rf 0.26 (hexane/EtOAc=6:4).). 1H NMR δ (DMSO-d6) 5.41 (s, 1H), 5.61 (s, 1H), 5.93 (s, 1H), 6.15 (s, 1H), 7.22 (m, 5H), 12.45 (s, 1H). [MH]− 177.2: tR=1.28 min; purity: 88%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794510B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-436c01d792854a81a420b18e82f41e2c |
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| Source note | uspto-grants-2004_09 |
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