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HRID 323756作成日:2026年10月25日

Water → 2-Cyclopropoxy-5-(trifluoromethoxy)benzaldehyde

https://huagongshe.com/reaction/323756

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Lithium naphthalenideHCID 11768624—
反応物2-(1-Phenylthiocycloprop-1-yl)oxy-5-(trifluoromethoxy)benzaldehydeHCID 21584078—
溶媒TetrahydrofuranHCID 8028—
生成物2-Cyclopropoxy-5-(trifluoromethoxy)benzaldehydeHCID 215840766%

反応手順

Freshly cut lithium metal (97 mg, 13.9 mmol) was added to a solution of naphthalene (1.77 g, 13.9 mmol) in THF (20 mL) and the mixture was sonicated at room temperature for 30 min. to produce a dark green solution of lithium naphthalenide. A solution of 2-(1-phenylthiocycloprop-1-yl)oxy-5-(trifluoromethoxy)benzaldehyde (Description 1, 96 mg, 0.27 mmol) in THF (2 mL) was cooled to −78° C. and the solution of lithium naphthalenide in THF (2 mL) was added dropwise until the intense green colour persisted. The reaction was then stirred for 5 min., water (6 mL) was added and the mixture was warmed to room temperature. The mixture was extracted with ethyl acetate, the combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with hexane/Et2O (80:20), to give to give the title compound as a colourless oil (4 mg, 6%). 1H NMR (360 MHz, CDCl3) δ0.86 (4H, m), 3.82-3.9 (1H, m), 7.42 (2H, m), 7.62 (1H, d, J 2.5 Hz), and 10.36 (1H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06214846B1
出典データセットuspto-grants-2001_04
ORD IDord-0fd22635a1df41eb8cf9f9ab6a49a840
出典メモuspto-grants-2001_04