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HRID 50471Erstellt: 26. Oktober 2026

Acetic Acid → N-(3-nitrophenyl)-3-(1,1,2,2-tetrafluoroethoxy)benzenemethanamine

https://huagongshe.com/reaction/50471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt3-NitroanilineHCID 7423—
EduktBenzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,1-DichloroethaneHCID 6365—
ProduktN-(3-nitrophenyl)-3-(1,1,2,2-tetrafluoroethoxy)benzenemethanamineHCID 2350609370%

Reaktionsschritte

EX-528A) 3-nitroaniline (1.87 g, 13.51 mmol) and 3-(1,1,2,2-tetrafluoroethoxy)-benzaldehyde (3 g, 13.5 mmol) were dissolved in 25 mL of dichloroethane and acetic acid (0.85 mL, 14.9 mmol), then solid NaBH(OAc)3 (3.73 g, 17.6 mmol) was added. The mixture was stirred at room temperature for 48 hours, then quenched with aqueous saturated sodium bicarbonate and diluted with ethyl acetate. The organic layer was dried over MgSO4, and concentrated in vacuo. The crude product was purified by flash column chromatography on silica gel eluting with ethyl acetate:hexane 1:7 to give 3.25 g (70%) of the desired N-(3-nitrophenyl)-3-(1,1,2,2-tetrafluoroethoxy) benzenemethan-amine product as a brown oil. HRMS calcd. for C15H13F4N2O3:345.0862 [M+H]+, found: 345.0864. 1H NMR (CDCl3) δ 4.4 (s, 2H), 4.5 (s, 1H), 5.9 (tt, 1H), 6.9 (d, 1H), 7.1 (d, 1H), 7.2-7.3 (m, 3H), 7.4 (m, 2H), 7.5 (d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710089B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-12d2c30d999341bfae347799e008c7e6
Quellennotizuspto-grants-2004_03