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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 577472Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonyl chlorideHCID 31297—
EduktBoron, trifluoro(methanol)-, (T-4)-HCID 11062313—
EduktHCID 89350921HCID 89350921—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-Methoxy-3,4-dihydroisoquinolin-1(2H)-oneHCID 13521672117,1%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040515B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-5ea636e0cd3f4155a2a87985ff4141c0
Quellennotizuspto-grants-2015_05