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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839476Generated: November 1, 2026

Acetic Acid → HCID 10281896, compound

https://huagongshe.com/reaction/1839476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(3-trifluoromethoxyphenoxy)anilineHCID 10880118—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 10281896HCID 10281896165.6%

Reaction Steps

EX-19C) To a solution of 3-(3-trifluoromethoxyphenoxy)aniline (1.0 g, 3.7 mmol) from EX-19B and 3-(1,1,2,2-tetrafluoroethoxy)benzaldehyde (0.83 g, 3.7 mmol) in 18.5 mL of dichloroethane was added sodium triacetoxyborohydride (1.0 g, 4.7 mmol) and glacial acetic acid (0.25 mL, 4.3 mmol). The reaction mixture was stirred at room temperature overnight then quenched with saturated aqueous sodium bicarbonate and extracted with methylene chloride. The organic layer was dried over MgSO4 and concentrated in vacuo to give 1.8 g (100%) of the desired [3-(3-trifluoromethoxy-phenoxy)phenyl][[3-(1,1,2,2-tetrafluoroethoxy)phenyl]methyl]amine product as a yellow oil, which was greater than 90% pure by reverse phase HPLC analysis. HRMS calcd. for C22H16F7NO3: 476.1097 [M+H]+, found: 476.1069. This material was carried on to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677341B2
Source datasetuspto-grants-2004_01
ORD IDord-bc2df1bd032e4aaba11f02ed35fddf57
Source noteuspto-grants-2004_01