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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990535Generated: October 26, 2026

Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)- → 3-(3-Phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl)oxazolidine

https://huagongshe.com/reaction/990535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
Reactant3-[(n-3-Phenoxy-phenyl)amino]1,1,1-trifluoro-2-propanolHCID 23506063—
SolventTolueneHCID 1140—
Product3-(3-Phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl)oxazolidineHCID 1011784592%

Reaction Steps

A toluene solution (5 mL) of 3-(1,1,2,2-tetrafluoroethoxy)benzaldehyde (0.45 g, 2.0 mol) and N-(3-phenoxyphenyl)-3-amino-1,1,1-trifluoro-2-propanol (0.60 g, 2.0 mmol) was refluxed in the presence of molecular sieves and Znl2 (˜5 mg) for 18 h under N2. The reaction mixture was filtered to remove the sieves, and the filtrate was diluted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and evaporated to give 0.92 g (92%) of the desired 3-(3-phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl)oxazolidine product as a colorless oil. The formation of the desired product was monitored by the disappearance of the aldehyde peak (δ10) in the 1H NMR spectrum. HRMS calcd. 502.1253 [M+H]+, found: 502.1220.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458852B1
Source datasetuspto-grants-2002_10
ORD IDord-8b036a2d00ee428ab738b6992a70418c
Source noteuspto-grants-2002_10