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HRID 227411作成日:2026年10月26日

7-(Benzyloxy)-1H-indole → (7-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanone

https://huagongshe.com/reaction/227411

反応式

関与物質

役割名称HCID仕込み量
反応物7-(Benzyloxy)-1H-indoleHCID 260798—
反応物2,2,3,3-Tetramethylcyclopropane-1-carbonyl chlorideHCID 11041002—
反応物HCID 178418443HCID 178418443—
触媒ZincchlorideHCID 3007855—
溶媒DichloromethaneHCID 6344—
生成物(7-Benzyloxy-1H-indol-3-yl)-(2,2,3,3-tetramethyl-cyclopropyl)-methanoneHCID 2482447640%

反応手順

A mixture of 7-benzyloxyindole (Matrix Scientific, 2.0 g, 9.0 mmol), ethylmagnesium bromide (1.0 M solution in THF, 11 mL, 11 mmol), zinc chloride (1.0 M solution in Et2O, 11 mL, 11 mmol) and the product of Example 1A (13.4 mmol) in 30 mL of dichloromethane was processed as described in Example 1B to provide the title compound (1.3 g, 3.6 mmol, 40% yield). MS (DCI/NH3) m/z 348 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560481B2
出典データセットuspto-grants-2009_07
ORD IDord-ecde1ad6124448cb93b342494b888b95
出典メモuspto-grants-2009_07