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HRID 50468Erstellt: 24. Oktober 2026

Acetic Acid → Ethyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoate

https://huagongshe.com/de/reaction/50468

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1,1-DichloroethaneHCID 6365—
EduktEthyl 3-aminobenzoateHCID 11400—
EduktBenzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
EduktSodium triacetoxyborohydrideHCID 5049666—
ProduktEthyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoateHCID 2350605299,9%

Reaktionsschritte

EX-456A) Ethyl 3-aminobenzoate (6.75 mL, 0.045 mol) and 3-(1,1,2,2-tetrafluoro-ethoxy)benzaldehyde (10 g, 45 mmol) were dissolved in 100 mL. of dichloroethane and acetic acid (2.7 mL, 47 mmol), then solid NaBH(OAc)3 (14.3 g, 67 mmol) was added. The mixture was stirred at room temperature for 3 hours, then quenched with aqueous sodium bicarbonate and extracted with dichloromethane. The organic layer was washed with brine, then dried over MgSO4, and evaporated to give 16.7 g (98%) of the desired ethyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoate product as a yellow oil. 1H NMR (CDCl3) δ 1.3 (t, 3H), 4.3 (q, 2H), 4.5 (s, 2H), 6.5 (tt, 1H), 6.9 (d, 1H), 7.1-7.4 (m, 7H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710089B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-36cec2421c9946a5ae83edbbd1f2758d
Quellennotizuspto-grants-2004_03