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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462491Generated: November 1, 2026

Hydrogen Bromide → HCID 178510788, compound

https://huagongshe.com/reaction/1462491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantPhenolHCID 996—
Reactant(2-Amino-3-phenylpropyl)phosphonic acidHCID 12749378—
ReactantHCID 13145060HCID 13145060—
ReactantWater ammonium hydroxideHCID 86589665—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 178510788HCID 178510788—

Reaction Steps

A mixture of [2-[[(4-methylphenyl)sulfonyl]amino]-3-phenylpropyl]phosphonic acid, diethyl ester (5.9 g., 13.9 mmole), phenol (8.0 g., 85.1 mmole), and 48% aqueous hydrobromic acid (50 ml.) is refluxed for 5.5 hours. The cooled mixture is diluted with water (50 ml.) and washed with ethyl acetate (2×50 ml.). The aqueous phase is evaporated to dryness, taken up in water (30 ml.) and evaporated again. This is repeated twice more. Finally, the residue is taken up in water and applied to an AG 50 W-X2 (H+ form) column (60 ml. bed volume) and eluted first with water then with 5% pyridine-water. The fractions containing the desired product are combined and evaporated to dryness. The solid residue is triturated with acetonitrile to give 2.55 g. of (2-amino-3-phenylpropyl)phosphonic acid as an off-white crystalline solid; m.p. 347° (dec.); TLC (isopropanol/conc. NH4OH/water; 7:2:1) spot at Rf =0.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460579
Source datasetuspto-grants-1984_07
ORD IDord-7bc8d160f3574be98f3d9a2cd7ce787d
Source noteuspto-grants-1984_07