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HRID 2103455Erstellt: 23. Oktober 2026

Hydrochloric Acid → Methyl-3-aminomethyl-2-(methoxycarbonyl)benzoate hydrochloride

https://huagongshe.com/de/reaction/2103455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethyl 3-cyanobenzene-1,2-dicarboxylateHCID 21988554—
EduktHCID 178418361HCID 178418361—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
ProduktMethyl-3-aminomethyl-2-(methoxycarbonyl)benzoate hydrochlorideHCID 2198853890%

Reaktionsschritte

To a solution of methyl-3-cyano-2-(methoxycarbonyl)benzoate (12.3 g, 57 mmol) in methanol (250 ml) and 4N HCl (40 ml) was added 10% Pd/C (1.2 g). The mixture was hydrogenated under 50 psi of hydrogen in a Parr Type Shaker for 17 hours. The mixture was filtered through Celite and the filtrate was concentrated in vacuo. The residue was further evaporated with ethanol (2×25 ml) and toluene (25 ml) and dried under vacuum. The resulting solid was slurried in ether (50 ml) for 1 hour. The slurry was then filtered and dried to give 13.46 g (90%) of the product as a white solid: 1H NMR (DMSO-d6) δ 8.79 (b, 2H), 7.94 (d, J=7.8 Hz, 1H), 7.88 (d, J=7.7 Hz, 1H), 7.72 (t, J=7.7 Hz, 1H), 4.03 (s, 2H), 3.86 (s, 3H), 3.85 (s, 3H); 13C NMR (DMSO-d6) δ 167.58, 166.12, 133.41, 133.18, 132.28, 130.62, 129.49, 52.99, 52.92, 39.25.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07576104B2
Quelldatensatzuspto-grants-2009_08
ORD IDord-d6d5e9c8520e4d098d98a7b39a0a3246
Quellennotizuspto-grants-2009_08