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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 733216생성일: 2026년 10월 25일

N-Ethylphthalimide → 2-ethyl-3-hydroxy-1,3-dihydro-2H-isoindol-1-one

https://huagongshe.com/reaction/733216

반응식

참여 물질

역할이름HCID투입량
반응물N-EthylphthalimideHCID 21120—
용매MethanolHCID 887—
용매Potassium borohydrideHCID 4192641—
생성물2-ethyl-3-hydroxy-1,3-dihydro-2H-isoindol-1-oneHCID 1530591047%

반응 조건

온도20 °C

반응 단계

3-Hydroxy-2-ethyl-2,3-dihydroisoindol-1-one is prepared as described in Example 1, starting with 4.0 g of N-ethylphthalimide in 20 cm3 of methanol and 1.2 g of potassium borohydride. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours and is then cooled to a temperature in the region of 0° C. and distilled water is added dropwise. The precipitate obtained is filtered off and then washed with cold water. The methanol is then partially evaporated from the filtrate under reduced pressure (2 kPa) at a temperature in the region of 35° C., and the residue is cooled to 0° C. The second precipitate thus obtained is filtered off and then washed with cold water. The two fractions of solid are dried under reduced pressure (2 kPa) at a temperature in the region of 35° C. 1.9 g of 3-hydroxy-2-ethyl-2,3-dihydroisoindol-1-one are thus obtained in the form of a flaky white powder. (Rf=0.5, thin layer chromatography on silica gel, eluent: cyclohexane/ethyl acetate (30/70 by volume)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07589117B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-7539f4e08ff74215a8cb335e7b8b9f2b
출처 메모uspto-grants-2009_09