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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10899생성일: 2026년 10월 23일

Toluene-p-sulphonic anhydride → Allyl 2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate

https://huagongshe.com/ko/reaction/10899

반응식

참여 물질

역할이름HCID투입량
반응물Toluene-p-sulphonic anhydrideHCID 77773—
반응물Allyl 3-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionateHCID 21982185—
용매Propan-2-one--water (1/1)HCID 18366337—
생성물Allyl 2-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrateHCID 21982199—

반응 조건

온도80 °C

반응 단계

Allyl 3-(4-fluoro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate (331 mg, 0.91 mmol) was dissolved in a a solvent mixture of acetone/water (v/v=5/1), and catalyst amount of p-toluenesulfonic acid anhydride was added to the obtained solution. The resulting mixture was refluxed at 80° C. for 18 hours. After the reaction was completed, the reaction mixture was washed with water, and then acetone was removed by distilling under a reduced pressure. The residue was extracted with dichloromethane. The combined organic layer was dried with anhydrous sulfate and distilled under a reduced pressure. The desired product was obtained (131.2 mg, 31%) by performing column chromatography (eluent: n-hexane/ethyl acetate=2/1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094908B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-dbb505f7b1a54d5491bd553456441248
출처 메모uspto-grants-2006_08