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HRID 273957作成日:2026年10月25日

Acetic Anhydride → 3(-1-Acetoxytridecyl)-4-phenylfuran

https://huagongshe.com/reaction/273957

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物4-Phenyl-3-furaldehydeHCID 15037148—
反応物HCID 178443215HCID 178443215—
溶媒TetrahydrofuranHCID 8028—
生成物3(-1-Acetoxytridecyl)-4-phenylfuranHCID 15037156—

反応手順

Dodecylmagnesium bromide (a 1.0M solution in THF; 2.11 ml, 2.11 mmol) was added to a solution of 4-phenyl-3-furaldehyde (303 mg, 1.76 mmol) in THF at 0 degrees under argon and gradually allowed to warm to room temperature with stirring. When all of the aldehyde was consumed acetic anhydride (719 mg, 7.04 mmol) was added and stirring was continued for 2 hours more. The reaction was quenched with saturated ammonium chloride and the organics were extracted into ethyl ether. The combined fractions were washed with saturated sodium bicarbonate, water and brine, dried over magnesium sulfate and concentrated to a yellow oil which was purified by flash chromatography on silica using 3% ethyl ether hexanes to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387606
出典データセットuspto-grants-1995_02
ORD IDord-b1812e3a919a44a88201410d57a6b28c
出典メモuspto-grants-1995_02