HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54912Generated: October 27, 2026
Water → Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate
https://huagongshe.com/reaction/54912
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Tetraisopropyl methylenediphosphonate | HCID 74266 | — |
| Reactant | (2E,6E)-1-bromo-3,7,11-trimethyldodeca-2,6,10-triene | HCID 5366048 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate | HCID 86750760 | 60.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05624917 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-73a7b1d009aa461cb31c197a6b725fa7 |
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| Source note | uspto-grants-1997_04 |
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