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HRID 733216作成日:2026年10月26日

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

https://huagongshe.com/reaction/733216

反応式

関与物質

役割名称HCID仕込み量
反応物N-EthylphthalimideHCID 21120—
溶媒MethanolHCID 887—
溶媒Potassium borohydrideHCID 4192641—
生成物2-ethyl-3-hydroxy-1,3-dihydro-2H-isoindol-1-oneHCID 1530591047%

反応条件

温度20 °C

反応手順

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)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07589117B2
出典データセットuspto-grants-2009_09
ORD IDord-7539f4e08ff74215a8cb335e7b8b9f2b
出典メモuspto-grants-2009_09