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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991330Generated: 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/991330

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 (δ10) in the 1H NMR spectrum. HRMS calcd. 502.1253 [M+H]+, found: 502.1220.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462092B1
Source datasetuspto-grants-2002_10
ORD IDord-37ab9ffafd3f46fea18e2925121d83e7
Source noteuspto-grants-2002_10