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HRID 1736524생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1736524

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물4-Phenyl-3-furaldehydeHCID 15037148—
반응물HCID 178443215HCID 178443215—
용매TetrahydrofuranHCID 8028—
생성물3(-1-Acetoxytridecyl)-4-phenylfuranHCID 15037156—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05541221
출처 데이터셋uspto-grants-1996_07
ORD IDord-1c890a15d45e4f7cb7939955810b5e01
출처 메모uspto-grants-1996_07