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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 577471Erstellt: 26. Oktober 2026

Triethylamine → [(E)-(6-methoxy-2,3-dihydroinden-1-ylidene)amino] methanesulfonate

https://huagongshe.com/reaction/577471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
EduktOxime-2,3-dihydro-6-methoxy-1H-inden-1-oneHCID 11389720—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt[(E)-(6-methoxy-2,3-dihydroinden-1-ylidene)amino] methanesulfonateHCID 8935092167%

Reaktionsschritte

To a solution of (1E)-N-hydroxy-6-methoxy-2,3-dihydro-1H-inden-1-imine (1a, 28.0 g, 158 mmol), DMAP (1.93 g, 15.8 mmol) and Et3N (63.8 g, 632 mmol) in dry DCM (200 mL) was added MsCl (27.5 g, 239 mmol) dropwise at 0° C. After the addition, the resulting solution was stirred at room temperature for 14 hours. The reaction mixture was washed with water (150 mL), saturated NH4Cl (130 mL) and brine (130 mL). The organic layer was dried over Na2SO4 and concentrated under vacuum. The residue was purified by column chromatography (petroleum ether/EtOAc, 1:1) to give (1E)-6-methoxy-N-[(methylsulfonyl)oxy]-2,3-dihydro-1H-inden-1-imine (1b, 27 g, 67%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040515B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-3db53b1a8b7f4c048c51a3a1cde3d096
Quellennotizuspto-grants-2015_05