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HRID 1039297作成日:2026年10月27日

Acetonitrile → (8-Hydroxy-7-isopropyl-2-methyl-7,8-dihydro-6H-indeno[5,4-d][1,3]oxazol-8-yl)acetonitrile

https://huagongshe.com/reaction/1039297

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物HexamethyldisilazaneHCID 13838—
反応物7-Isopropyl-2-methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-oneHCID 57781252—
反応物HCID 178418244HCID 178418244—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
溶媒Ammonium ChlorideHCID 25517—
生成物(8-Hydroxy-7-isopropyl-2-methyl-7,8-dihydro-6H-indeno[5,4-d][1,3]oxazol-8-yl)acetonitrileHCID 5778123680%

反応手順

To a solution of 1,1,1,3,3,3-hexamethyldisilazane (917 mg, 5.68 mmol) in tetrahydrofuran (10 mL) was added 1.6M butyllithium/hexane solution (3.55 mL, 5.68 mmol) at −78° C., and the mixture was stirred for 15 min. Thereto was added a solution of acetonitrile (313 μL, 5.95 mmol) in tetrahydrofuran (2 mL), and the mixture was stirred for 30 min. Then, a solution of 7-isopropyl-2-methyl-6,7-dihydro-8H-indeno[5,4-d][1,3]oxazol-8-one (650 mg, 2.84 mmol) in tetrahydrofuran (2 mL) was added. After stirring for 30 min, the reaction solution was diluted with saturated aqueous ammonium chloride solution and ethyl acetate, washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80→100/0) to give the title compound (614 mg, yield 80%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08552037B2
出典データセットuspto-grants-2013_10
ORD IDord-a785a423bee743438c5024c4c9488589
出典メモuspto-grants-2013_10