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HRID 990428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/990428

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—
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 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 (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US06458803B1
出典データセットuspto-grants-2002_10
ORD IDord-285d96e9ac4f4586b170851393c18fa5
出典メモuspto-grants-2002_10