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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840180Generated: October 31, 2026

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

https://huagongshe.com/reaction/1840180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantBenzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,1-DichloroethaneHCID 6365—
ProductEthyl 3-[[[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amino]benzoateHCID 2350605299.9%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677379B2
Source datasetuspto-grants-2004_01
ORD IDord-13e6d7c825dd4221b64f919ab777726d
Source noteuspto-grants-2004_01