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HRID 326372作成日:2026年10月25日

Dodecanoyl chloride → 4-Dodecoyloxymethyl-3-phenyl-2-triethylsilylfuran

https://huagongshe.com/reaction/326372

反応式

関与物質

役割名称HCID仕込み量
反応物Dodecanoyl chlorideHCID 8166—
反応物TriethylamineHCID 8471—
反応物3-Phenyl-2-triethylsilyl-4-furanmethanolHCID 15037150—
溶媒TetrahydrofuranHCID 8028—
生成物4-Dodecoyloxymethyl-3-phenyl-2-triethylsilylfuranHCID 15037151—

反応手順

To a stirred solution of 3-phenyl-2-triethylsilyl-4-furanmethanol (345 mg, 1.20 mmol) and triethylamine (182 mg, 1.80 mmol) in tetrahydrofuran (15 ml) at 0 degrees under argon was added lauroyl chloride (786 mg, 3.60 mmol). This solution was allowed to warm gradually to room temperature. After stirring an additional 2 hours the white precipitate was filtered off. The filtrate was taken up into ethyl ether, washed with saturated ammonium chloride, saturated sodium bicarbonate, H2O and brine. Evaporation of the dried (magnesium sulfate) extracts gave an oil which was purified by flash chromatography on silica using 2% ethyl ether/hexanes to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05268387
出典データセットuspto-grants-1993_12
ORD IDord-e319edf6999c4c0b9e0d6b27c6e90b99
出典メモuspto-grants-1993_12