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HRID 1376967作成日:2026年10月27日

Pentane → 5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran

https://huagongshe.com/reaction/1376967

反応式

関与物質

役割名称HCID仕込み量
反応物PentaneHCID 8003—
反応物Heptyltriphenylphosphonium bromideHCID 2724567—
反応物5-Benzyloxy-4-t-butyl-2-formylbenzofuranHCID 23442879—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuranHCID 5430872291.2%

反応手順

A pentane solution (2.6 ml, 4.2 mmol) of 1.6M n-butyllithium was added dropwise to a solution of n-heptyltriphenylphosphonium 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%)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05663373
出典データセットuspto-grants-1997_09
ORD IDord-8f9839940081438eb9ea5381c16840c8
出典メモuspto-grants-1997_09