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HRID 133437Erstellt: 25. Oktober 2026

Methanamine, N-methoxy-, hydrochloride (1:1) → N-Methoxy-N-methyl-3-(4-chlorophenyl)-2-(3-fluorophenyl)propanamide

https://huagongshe.com/reaction/133437

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
EduktMethyl 3-(4-chlorophenyl)-2-(3-fluorophenyl)propionateHCID 16098347—
EduktDimethylalumanylium chlorideHCID 16686359—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-Methoxy-N-methyl-3-(4-chlorophenyl)-2-(3-fluorophenyl)propanamideHCID 16098351—

Reaktionsschritte

To a suspension N-methoxy-N-methylamine hydrochloride (2.0 g, 21 mmol) in 50 mL CH2Cl2 at 0° C. was added dimethylaluminum chloride (1 M in hexane, 21 mL, 21 mmol). After stirring at room temperature for 1 h, a solution of methyl 3-(4-chlorophenyl)-2-(3-fluorophenyl)propionate (Step A, 2.0 g, 10 mmol) in CH2Cl2 (10 mL) was added, and the resulting mixture was stirred overnight. The reaction mixture was quenched by addition of MeOH (5 mL), and the resulting mixture was concentrated with silica gel (50 g). The material was loaded onto a silica gel column, which was eluted with 10% EtOAc in hexane to 2% ammonia in MeOH (2 M) in 10% EtOAc/hexane to give the title compound. 1H NMR (400 MHz, CD3OD): δ 7.35-6.90 (m, 8H), 4.39 (br, 1H), 3.41 (s, 3H), 3.38-3.30 (m, 1H), 3.08 (s, 3H), 2.92 (dd, 1H). LC-MS: m/e 322 (M+H)+ (3.6 min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390835B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-bdb3a302d9924d91aa890ebc3c4f8da6
Quellennotizuspto-grants-2008_06