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HRID 374953作成日:2026年10月26日

Dimethylformamide → 2,3-Dichloro-6-fluorobenzaldehyde

https://huagongshe.com/reaction/374953

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物CyclohexaneHCID 8078—
反応物1,2-Dichloro-4-fluorobenzeneHCID 74028—
反応物Acetone cardiceHCID 18522661—
反応物CID 53628100HCID 178418400—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2,3-Dichloro-6-fluorobenzaldehydeHCID 3260062—

反応条件

温度-45 °C

反応手順

A solution of 1.3M s-butyl lithium in cyclohexane (244 mL, 317 mmol) is added to a dry-ice/acetone cooled solution of TMEDA (34 g, 293 mmol) in THF (250 mL), maintaining the internal reaction temperature <-70° C. The resulting reaction mixture is cooled and maintained at ≤-90° C. with an ether/liquid nitrogen bath while a solution of 1,2-dichloro-4-fluorobenzene (40 g, 244 mmol) in THF (100 mL) is added dropwise. The resulting reaction mixture is stirred with dry-ice/acetone cooling for 1h, then is cannulated into an ether/liquid nitrogen cooled and mechanically stirred solution of DMF (89.1 g, 1.22 mol) in THF (125 mL). The resulting mixture is warmed to -45° C. and partitioned between dilute aqueous HCl and ether. The organic solution is washed with aqueous NaHCO3, dried (MgSO4), and concentrated to afford 44.38 g of 2-fluoro-5,6-dichlorobenzaldehyde as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05482974
出典データセットuspto-grants-1996_01
ORD IDord-c71469b9738f4ef7aae2f3a53f0962d6
出典メモuspto-grants-1996_01