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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881822Generated: October 26, 2026

Sodium Hydroxide → (R)-4-(biphenyl-4-yl)-3-(3-carboxypropanamido)butanoic acid

https://huagongshe.com/reaction/881822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant(R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl esterHCID 49822223—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(R)-4-(biphenyl-4-yl)-3-(3-carboxypropanamido)butanoic acidHCID 5960766796.6%

Reaction Steps

To a solution of (R)-4-(1-(biphenyl-4-yl)-4-ethoxy-4-oxobutan-2-ylamino)-4-oxobutanoic acid (61.2 mg, 0.160 mmol) in THF (1.6 mL) and methanol (0.2 mL), aqueous 1M NaOH solution (0.638 mL, 0.638 mmol) is added at room temperature. After stirring for 45 minutes, the reaction is quenched with aqueous 0.1 M HCl and is extracted with ethyl acetate. The organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give (R)-4-(biphenyl-4-yl)-3-(3-carboxypropanamido)butanoic acid (54.9 mg). HPLC retention time=1.33 minutes (condition A); MS (m+1)=356.1; 1H NMR (400 MHz, CD3OD) δ ppm 2.40-2.56 (m, 6 H) 2.83-2.94 (m, 2 H) 4.43-4.50 (m, 1 H) 7.29-7.32 (m, 3 H) 7.41 (t, 2 H, J=7.7 Hz) 7.53-7.60 (m, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993631B2
Source datasetuspto-grants-2015_03
ORD IDord-0ed18c4fe0c44f5b97536b74e4931e03
Source noteuspto-grants-2015_03