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HRID 1964148Erstellt: 25. Oktober 2026

Hydrochloric Acid → 7-Methoxy-8-methyl-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-one

https://huagongshe.com/reaction/1964148

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethyl AcrylateHCID 7294—
EduktTetrahydrofuranHCID 8028—
Eduktethyl 5-methoxy-4-methyl-1H-indole-2-carboxylateHCID 21396313—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTolueneHCID 1140—
Produkt7-Methoxy-8-methyl-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-oneHCID 67249703—

Reaktionsschritte

To a suspension of ethyl 5-methoxy-4-methyl-1H-indole-2-carboxylate (712 mg, 3.05 mmol) in toluene (10 mL) was added a 1 M solution of KOtBu in THF (3.97 mL, 3.97 mmol). The reaction mixture was stirred at room temperature for 5 min, methyl acrylate (825 μL, 9.15 mmol) was added. The reaction was stirred at reflux overnight and neutralized with 1 N HCl aqueous solution. The solid was collected and divided into three microwave vial. Each was added AcOH (8 mL) and H2O (1 mL), and heated at 180° C. for 15 min under microwave irradiation. The solvent was evaporated and the residue was purified by silica gel column chromatography to give the title compound as a yellow solid (500 mg). LCMS m/z=216.2 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 2.45 (s, 3H), 3.21 (t, J=6.5 Hz, 2H), 3.68 (s, 3H), 4.40 (t, J=6.2 Hz, 2H), 6.98 (s, 1H), 7.13 (d, J=9.0 Hz, 1H), 7.23 (d, J=9.0 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08415484B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-4b2174b178f749b4a68e483d51cceec3
Quellennotizuspto-grants-2013_04