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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54912Generated: October 27, 2026

Water → Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate

https://huagongshe.com/reaction/54912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantTetraisopropyl methylenediphosphonateHCID 74266—
Reactant(2E,6E)-1-bromo-3,7,11-trimethyldodeca-2,6,10-trieneHCID 5366048—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductTetraisopropyl (E,E)-farnesylmethylenebisphosphonateHCID 8675076060.9%

Reaction Steps

Oily sodium hydride (60%, 0.24 g) was added to a solution of tetraisopropyl methylenebisphosphonate (3.44 g) in dimethoxyethane (25 ml). The mixture was stirred at room temperature for 1 hour. Then, a solution of (E,E)-farnesyl bromide (1.43 g) in dimethoxyethane (5 ml) was added dropwise at 0° C. The reaction mixture was stirred at room temperature for 1 hour, then poured into water and extracted with ethyl acetate. The organic layer was washed with water and dried (MgSO4), and then the solvent was distilled off under reduced pressure. The oily residue was subjected to column chromatography on silica gel. Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate (1.67 g, 60.9%) was obtained as an oil from the fractions obtained by elution with ethyl acetate-chloroform (1:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624917
Source datasetuspto-grants-1997_04
ORD IDord-73a7b1d009aa461cb31c197a6b725fa7
Source noteuspto-grants-1997_04