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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356757Generated: October 29, 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/1356757

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—
Catalystzinc(II)iodideHCID 9883512—
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 ZnI2 (˜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 (δ˜10) in the 1H NMR spectrum. HRMS calcd. 502.1253 [M+H]+, found: 502.1220.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586433B2
Source datasetuspto-grants-2003_07
ORD IDord-251f3c4aa1f0419badaa70a9120cb30c
Source noteuspto-grants-2003_07