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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092921Generated: October 30, 2026

HCID 86632034, compound → HCID 23582774, compound

https://huagongshe.com/reaction/1092921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86632034HCID 86632034—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 23582774HCID 2358277475%

Reaction Steps

Next, 0.64 g (1.19 mmol) of benzyl 2-(N-benzyloxycarbonylamino)-4-[butyl(phenyl)phosphono]butanoate was dissolved in 20 mL of a solvent mixture of methanol and water at 3:1 and mixed with 200 mg of 5% palladium-carbon and hydrogen gas was introduced for 75 minutes. The palladium-carbon was removed by Celite filtration and the filtrate was vacuum-concentrated. The residue was purified by medium pressure reversed-phase column chromatography ODS-S-50B. The column was eluted with a linear gradient of 30 to 60% methanol at a flow rate of 6 mL/min, and the fractions containing the compound eluted at 60% methanol were collected. The elution and purity of the compound were confirmed by TLC (BuOH/AcOH/H2O=5:2:2, ninhydrin coloration). After vacuum concentration, freeze drying was carried out to obtain 2-amino-4-[butyl(phenyl)phosphono]butanoic acid (0.28 g, yield 75%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129557B2
Source datasetuspto-grants-2012_03
ORD IDord-4e744b9e259d484f8050f2d511f33a66
Source noteuspto-grants-2012_03