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HRID 732321作成日:2026年10月23日

Hydrochloric Acid → 4,7-Ethano-2H-isoindole-1-carboxylic acid, 4,7-dihydro-, ethyl ester

https://huagongshe.com/ja/reaction/732321

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Ethyl isocyanoacetateHCID 533707—
反応物5,6-Di(benzenesulfonyl)bicyclo[2.2.2]oct-2-eneHCID 12778411—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物4,7-Ethano-2H-isoindole-1-carboxylic acid, 4,7-dihydro-, ethyl esterHCID 1211665980%

反応条件

温度0 °C

反応手順

The reaction system of a mixture liquid of 7.76 g (20 mmol) of the obtained 5,6-bis(phenylsulfonyl)-bicyclo[2.2.2]octa-2-ene and 50 ml of anhydrous tetrahydrofuran was purged with nitrogen, and 2.425 ml (22 mmol) of ethyl isocyanoacetate was added to the system then cooled to 0° C. After dropping potassium t-butoxide (50 ml/1 M THF solution) over 2 hours, the solution was stirred for 3 hours. After the reaction was finished, dilute hydrochloric acid was added. The reaction mixture was then washed in turn with saturated aqueous sodium bicarbonate solution, distilled water and saturated saline, and dried over anhydrous sodium sulfate. The resulting product was purified using silica gel column chromatography (chloroform) to give ethyl-4,7-dihydro-4,7-ethano-2H-isoindole-1-carboxylate (3.5 g, 1.6 mmol, yield 80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07586117B2
出典データセットuspto-grants-2009_09
ORD IDord-ceb984c1462c428aa479ebf92d868891
出典メモuspto-grants-2009_09