참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Tetraisopropyl methylenediphosphonate | HCID 74266 | — |
| 반응물 | (2E,6E)-1-bromo-3,7,11-trimethyldodeca-2,6,10-triene | HCID 5366048 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | Tetraisopropyl (E,E)-farnesylmethylenebisphosphonate | HCID 86750760 | 60.9% |
반응 단계
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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05624917 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-73a7b1d009aa461cb31c197a6b725fa7 |
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| 출처 메모 | uspto-grants-1997_04 |
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