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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116816Generated: October 27, 2026

Methane → Zoledronic Acid

https://huagongshe.com/reaction/2116816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantDiphenyl EtherHCID 7583—
ReactantPhosphorus trichlorideHCID 24387—
ReactantPhosphorous acidHCID 107909—
Reactant(1-Imidazoyl)ethanoic acidHCID 17805625—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductZoledronic AcidHCID 68740—

Reaction Conditions

Temperature70 °C

Reaction Steps

The suspension of (1-imidazoyl)ethanoic acid (10.0 g) and phosphorous acid (19.5 g) in diphenyl ether (50 ml) was heated up to 70° C. for 1 hour. Phosphorous trichloride (20 ml) was slowly added to reaction mass at 70° C. temperature and maintained reaction temperature for another 6 hours. Reaction mass was cooled to 25° C. followed by addition of water (150 ml) and toluene (30 ml). Reaction mixture was again heated to 70° C. and charged charcoal in hazy biphasic solution, stirred, filtered through Hyflo bed, washed the bed with hot water (30 ml). Layers was separated from filtrate, aqueous layer was washed with toluene (20 ml) and combined organic layer was then back extracted with water (20 ml) and mixed with main aqueous layer. The water (140 ml) was distilled out from combined aqueous layer at atmospheric pressure in 2 hours and then refluxed the concentrated mass for 13 hours. Reaction mass was cooled to 25° C. followed by addition of methanol (50 ml) in 1 hours. The reaction mixture was stirred and again cooled to 0° C. followed filtration. The filtrate was washed with chilled 1:2 mixture (30 ml) of water and methanol and dried at 60° C. to get Zoledronic Acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439385B2
Source datasetuspto-grants-2008_10
ORD IDord-208c9159b7594b4592609475978b7503
Source noteuspto-grants-2008_10