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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272319생성일: 2026년 10월 26일

Phthalic Anhydride → 2-[2,2,4,6,7-Pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/272319

반응식

참여 물질

역할이름HCID투입량
반응물Phthalic AnhydrideHCID 6811—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium HydroxideHCID 14798—
반응물Sodium AcetateHCID 517045—
반응물2,2,4,6,7-Pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amineHCID 10685309—
용매TetrahydrofuranHCID 8028—
생성물2-[2,2,4,6,7-Pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-yl]-1H-isoindole-1,3(2H)-dioneHCID 2196132481%

반응 단계

To a solution of phthalic anhydride (566.4 mg, 3.82 mmol) in tetrahydrofuran (5 ml) was added a solution of 2,2,4,6,7-pentamethyl-3-(4-methylphenyl)-2,3-dihydro-1-benzofuran-5-amine (987.3 mg, 3.38 mmol) in tetrahydrofuran (10 ml) and the resulting mixture was refluxed with heating for 11 hours. The reaction mixture was cooled down to room temperature and then concentrated under reduced pressure. Sodium acetate (314.6 mg, 3.84 mmol) and acetic anhydride (20 ml) were added into the residue and the resulting mixture was stirred at 90° C. for 2 hours. The reaction mixture was cooled down to room temperature and then an 8 N aqueous solution of sodium hydroxide was added into the mixture until it became basic. The product was extracted twice with ethyl acetate. The combined extracts were washed with an aqueous saturated solution of sodium hydrogen carbonate, dried on magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was crystallized from ethyl acetate to obtain 1.16 g (81% yield) of the title compound. Melting point: 222-224° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456162B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-edb08aaaba004840be502a91438ba444
출처 메모uspto-grants-2008_11