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HRID 128747作成日:2026年10月26日

Tetrahydrofuran → trans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dione

https://huagongshe.com/reaction/128747

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物N-CarbethoxyphthalimideHCID 31187—
反応物Sodium BicarbonateHCID 516892—
反応物(1s,4s)-4-Aminocyclohexan-1-ol hydrochlorideHCID 522619—
溶媒WaterHCID 962—
生成物trans-2-(4-Hydroxycyclohexyl)-isoindole-1,3-dioneHCID 28872672.4%

反応手順

A solution of 4-aminocyclohexanol hydrochloride (6.08 g, 0.04 mole) in water (60 ml) was brought to pH 8 with aqueous sodium bicarbonate solution. N-carbethoxy-phthalimide (8.76 g, 0.04 mole) was added followed by tetrahydrofuran (until homogenous solution was obtained). The clear solution was stirred at room temperature overnight. During this time a white solid was precipitated. The tetrahydrofuran was removed in vacuo and the remaining aqueous solution was extracted with ethyl acetate until the solution was clear. The ethyl acetate extracts were combined, washed with water, dried (MgSO4) and concentrated to give 4-phthalimido cyclohexanol as a white solid (7.1 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464864
出典データセットuspto-grants-1995_11
ORD IDord-8ec7e128fb84498fa001bb7b74ba420b
出典メモuspto-grants-1995_11