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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386433Generated: October 30, 2026

Sodium Hydroxide → 3-(4-Phenoxyphenyl)propanoic acid

https://huagongshe.com/reaction/386433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-(4-phenoxyphenyl)propanoateHCID 20213313—
SolventMeOH tetrahydrofuranHCID 21899815—
Product3-(4-Phenoxyphenyl)propanoic acidHCID 22036572—

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of ethyl 3-(4-phenoxyphenyl)propanoate (S29, 500 mg, 1.95 mmol) in THF/MeOH (1/1, 8 mL) was treated with aqueous 4 N NaOH (0.5 mL) and was stirred for 20 h at 25° C. The reaction mixture was concentrated, diluted with aqueous 1 N HCl and extracted with CH2Cl2. The organic layer was dried over Na2SO4, filtered and concentrated to afford S30 (390 mg, 1.61 mmol, 82%) as a white solid: 1H NMR (CDCl3, 500 MHz) 7.34 (dd, 2H, J=8.4, 7.4 Hz), 7.18 (d, 2H, J=8.4 Hz), 7.10 (dt, 1H, J=7.7, 1.1 Hz), 7.00 (dd, 2H, J=8.8, 1.1 Hz), 6.95 (d, 2H, J=8.4 Hz), 2.96 (t, 2H, J=7.7 Hz), 2.70 (t, 2H, J=7.7 Hz); 13C NMR (CDCl3, 125 MHz) 179.2, 157.3, 155.6, 135.0, 129.7, 129.5, 123.1, 119.0, 118.7, 35.7, 29.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372823B2
Source datasetuspto-grants-2013_02
ORD IDord-6cafd303a38047b8b18091caf71cc16d
Source noteuspto-grants-2013_02