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HRID 50489作成日:2026年10月27日

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/50489

反応式

関与物質

役割名称HCID仕込み量
反応物Benzaldehyde, 3-(1,1,2,2-tetrafluoroethoxy)-HCID 118803—
反応物3-[(n-3-Phenoxy-phenyl)amino]1,1,1-trifluoro-2-propanolHCID 23506063—
触媒zinc(II)iodideHCID 9883512—
溶媒TolueneHCID 1140—
生成物3-(3-Phenoxyphenyl)-2-[3-(1,1,2,2-tetrafluoro-ethoxy)phenyl]-5-(trifluoromethyl)oxazolidineHCID 1011784592%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710089B2
出典データセットuspto-grants-2004_03
ORD IDord-7478c53abfe94783aaacc1978f318c02
出典メモuspto-grants-2004_03