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HRID 577472作成日:2026年10月24日

Methanesulfonyl chloride → 7-Methoxy-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/ja/reaction/577472

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物Boron, trifluoro(methanol)-, (T-4)-HCID 11062313—
反応物HCID 89350921HCID 89350921—
触媒Titanium TetrachlorideHCID 24193—
溶媒DichloromethaneHCID 6344—
生成物7-Methoxy-3,4-dihydroisoquinolin-1(2H)-oneHCID 13521672117.1%

反応手順

To a stirred suspension of (1E)-6-methoxy-N-[(methylsulfonyl)oxy]-2,3-dihydro-1H-inden-1-imine (1b, 27 g, 106 mmol), BF3/MeOH (14% in MeOH, 16.8 g, 170 mmol) and TiCl4 (32.3 g, 170 mmol) in dry DCM (200 mL) was added MsCl (20.9 g, 183 mmol) dropwise at 0° C. After the addition, the resulting solution was stirred at room temperature for 14 hours. To the reaction mixture was added DCM (200 mL) and the solution was washed with saturated NaHCO3 to pH ˜7. The organic layer was washed with brine (150 mL), dried over Na2SO4, and concentrated under vacuum. The residue was purified by column chromatography (DCM/MeOH) to give 7-methoxy-3,4-dihydroisoquinolin-1(2H)-one (1c, 22 g, 100%) as a gray solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040515B2
出典データセットuspto-grants-2015_05
ORD IDord-5ea636e0cd3f4155a2a87985ff4141c0
出典メモuspto-grants-2015_05