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HRID 20459作成日:2026年10月25日

Dimethylformamide → 3-Butyl-5-fluorobenzaldehyde

https://huagongshe.com/reaction/20459

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物1,3-Dibromo-5-fluorobenzeneHCID 137003—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物3-Butyl-5-fluorobenzaldehydeHCID 8623667943%

反応手順

Dissolve 1,3-Dibromo-5-fluoro-benzene (12.00 g, 0.05 mmol) in diethyl ether (470 mL) and cool to −78 C. Slowly add 1.6 M n-butyllithium in hexanes (29.5 mL, 49.6 mmol) and stir at −78 for one hour. Add dimethylformamide (3.45 g, 0.05 mmol) dropwise and warm to room temperature overnight. Quench with saturated aqueous ammonium chloride solution. Separate the layers and extract the organic layer (1×300 mL) with diethyl ether. Combine the organic layers and wash (1×150 mL) with water, (1×100 μL) with saturated aqueous sodium chloride and dry over magnesium sulfate. Purify using medium pressure chromatography (silica gel, 0-10% diethyl ether:hexanes) to give the desired product (4.15 g, 43%) as a yellow liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745438B2
出典データセットuspto-grants-2010_06
ORD IDord-c476a40dfe7e47f582869f13e0b36cae
出典メモuspto-grants-2010_06