참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pentane | HCID 8003 | — |
| 반응물 | Heptyltriphenylphosphonium bromide | HCID 2724567 | — |
| 반응물 | 5-Benzyloxy-4-t-butyl-2-formylbenzofuran | HCID 23442879 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran | HCID 54308722 | 91.2% |
반응 단계
A pentane solution (2.6 ml, 4.2 mmol) of 1.6M n-butyllithium was added dropwise to a solution of n-heptyl-triphenylphosphonium bromide (1.84 g, 4.2 mmol) in tetrahydrofuran (10 ml) under a nitrogen atmosphere. After stirring the mixture at room temperature for 30 min, a solution of 5-benzyloxy-4-tert-butyl-2-formylbenzofuran (1.0 g, 3.2 mmol) in tetrahydrofuran (10 ml) was added dropwise. Subsequently, the mixture was stirred at room temperature for 30 min, poured into ice water and subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and water, then dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (chloroform) to afford 5-benzyloxy-4-tert-butyl-2-(1-octenyl)benzofuran [1.14 g (yield, 91%)].
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05606089 |
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| 출처 데이터셋 | uspto-grants-1997_02 |
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| ORD ID | ord-0c524a98fa604ab28b3f3c9019a7cebd |
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| 출처 메모 | uspto-grants-1997_02 |
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