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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677616Generated: November 1, 2026

Sodium Hydroxide → 2-(3-Aminophenyl)-3-((4-phenylbutyl)(hydroxy)phosphinoyl)propanoic acid

https://huagongshe.com/reaction/1677616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-(3-(t-Butoxycarbonylamino)phenyl)-3-((4-phenylbutyl)(hydroxy)-phosphinoyl)propanoic acid methyl esterHCID 67375137—
SolventMethanol tetrahydrofuran waterHCID 21892291—
Product2-(3-Aminophenyl)-3-((4-phenylbutyl)(hydroxy)phosphinoyl)propanoic acidHCID 10126160—

Reaction Steps

2-(3-(t-Butoxycarbonylamino)phenyl)-3-((4-phenylbutyl)(hydroxy)-phosphinoyl)propanoic acid methyl ester (845 mg, 1.8 mmol) was stirred in 1 M NaOH (5.3 mL, 5.3 mmol) in methanol/THF/H2O for 1.5 hours. The product was concentrated in vacuo. The residue was dissolved in 10 mL methylene chloride and TFA (10 mL) was added. After 45 minutes, the reaction mixture was concentrated to provide 2-(3-aminophenyl)-3-((4-phenylbutyl)(hydroxy)phosphinoyl)propanoic acid, NMR (DMSO-d6) 1.30-1.45 (m, 8), 1.80 (m, 1), 2.35 (m, 1), 3.62 (m, 1), 6.58-6.65 (m, 3), 7.05 (m, 1), 7.15 (m, 3), 7.23 (m, 2) ppm; as a crude product. Pure product was obtained by preparative reversed-phase HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008325B2
Source datasetuspto-grants-2011_08
ORD IDord-7d0b3c0ce91b4993af4bd4d0157e0bac
Source noteuspto-grants-2011_08