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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092917Generated: November 3, 2026

Water → HCID 86632028, compound

https://huagongshe.com/reaction/1092917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAnisoleHCID 7519—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 86632029HCID 86632029—
SolventNitromethaneHCID 6375—
ProductHCID 86632028HCID 8663202857%

Reaction Steps

Next, 0.73 g (1.37 mmol) of benzyl 2-(N-benzyloxycarbonylamino)-4-[(4-chlorophenyl)(methyl)phosphono]butanoate and 0.89 g (8.22 mmol) of anisole were dissolved in 10 mL of dry nitromethane and mixed with 0.55 g (4.11 mmol) of aluminum trichloride. After stirring was carried out at room temperature for 1 hour, 20 mL of water was added and stirred for 10 minutes. The mixture was washed with 50 mL of ether three times and the water layer was separated and methanol was added to adjust the final concentration of methanol to be 30%. The solution was passed through a short column of neutral silica gel 60N to remove aluminum hydroxide. Without being concentrated, the eluent was purified by medium pressure reversed-phase column chromatography ODS-S-50B. The column was eluted with 40% methanol at a flow rate of 6 mL/min and the fractions of the compound 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-[(4-chlorophenyl)(methyl)phosphono]butanoic acid (0.24 g, yield 57%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129557B2
Source datasetuspto-grants-2012_03
ORD IDord-f77bf42df0274535a928dca399d46cf8
Source noteuspto-grants-2012_03