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HRID 54912作成日:2026年10月25日

Water → Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate

https://huagongshe.com/reaction/54912

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物Tetraisopropyl methylenediphosphonateHCID 74266—
反応物(2E,6E)-1-bromo-3,7,11-trimethyldodeca-2,6,10-trieneHCID 5366048—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物Tetraisopropyl (E,E)-farnesylmethylenebisphosphonateHCID 8675076060.9%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624917
出典データセットuspto-grants-1997_04
ORD IDord-73a7b1d009aa461cb31c197a6b725fa7
出典メモuspto-grants-1997_04