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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1893029생성일: 2026년 10월 25일

Diisopropylcarbodiimide → 6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic Acid Pentafluorophenyl Ester

https://huagongshe.com/reaction/1893029

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참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물PentafluorophenolHCID 13041—
반응물1,3-Dihydro-1,3-dioxo-2H-isoindole-2-hexanoic acidHCID 78185—
용매DichloromethaneHCID 6344—
생성물6-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-hexanoic Acid Pentafluorophenyl EsterHCID 59347289101.3%

반응 조건

온도0 °C

반응 단계

Referring to scheme 12, compound 41a (13.3 g, 51 mmol) was dissolved in anhydrous dichloromethane (40 mL) and cooled to 0° C. under argon. To the solution were added diisopropyl carbodiimide (6.31 g, 7.7 mL, 50 mmol) and pentafluoro phenol (42, 9.2 g, 50 mmol). After overnight the reaction mixture was evaporated to dryness. To the residue ethyl acetate (100 mL) was added and the filtered to remove diisopropyl urea. The precipitate was washed with ethyl acetate (50 mL). The combined organic layer was washed with saturated sodium bicarbonate and water. The organic layer was dried over sodium sulfate, filtered and evaporated to dryness. Compound 43a (Rf=0.8 in 10% EtOAc/Hexane, 21.65 g, 92%) was obtained, which was directly used for the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507661B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-04b44437682648cb98857172d8b96b0d
출처 메모uspto-grants-2013_08