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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1050458생성일: 2026년 10월 26일

Methanesulfonic Acid → Phthalimide

https://huagongshe.com/reaction/1050458

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물Acetic AnhydrideHCID 7918—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물2-(3-Oxobutyl)isoindoline-1,3-dioneHCID 290728—
용매Ethyl AcetateHCID 8857—
생성물PhthalimideHCID 680922.3%

반응 조건

온도70 °C

반응 단계

To a stirred solution of acetic anhydride (5.0 mL, 53.0 mmol) and 7.7 wt % phosphorus pentoxide in methanesulfonic acid (Eaton's Reagent) (5.0 mL, 4.60 mmol) was added 2-(3-oxobutyl)isoindoline-1,3-dione (1.0 g, 4.60 mmol). The reaction was heated at 70° C. and for 8 h. The reaction was allowed to cool to room temperature and maintained overnight. The reaction was diluted with EtOAc, washed with ice cold water, dried (Na2SO4), filtered and concentrated under vacuum. The residue was purified by silica gel chromatography (Analogix, SF40-115 g, 20-100% EtOAc in hexanes). The pure fractions were combined and evaporated to dryness and triturated with 10% EtOAc in hexanes, filtered and evaporated to dryness to give 2-(2,6-dimethyl-4-oxo-4H-pyran-3-yl)methyl)isoindoline-1,3-dione (290 mg, 1.024 mmol, 22.24% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 7.91-7.74 (m, 4 H), 6.06 (s, 1 H), 4.54 (s, 2 H), 2.43 (s, 3 H), 2.22 (s, 3 H). MS(ES) [M+H]+ 284.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09382234B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-86a81e7ba5e140e19d116f530394757f
출처 메모uspto-grants-2016_07