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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant(+)Methyl 3(S)-hydroxy-2-methylene-3-phenylpropanoateHCID 11008751—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3(S)-hydroxy-2-methylene-3-phenylpropanoic AcidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794510B2
Source datasetuspto-grants-2004_09
ORD IDord-436c01d792854a81a420b18e82f41e2c
Source noteuspto-grants-2004_09