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HRID 420329作成日:2026年10月26日

Hydrochloric Acid → 5-tert-Butyl-2-fluoro-benzaldehyde

https://huagongshe.com/reaction/420329

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DimethylformamideHCID 6228—
反応物HexaneHCID 8058—
反応物1-(1,1-Dimethylethyl)-4-fluorobenzeneHCID 136540—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物5-tert-Butyl-2-fluoro-benzaldehydeHCID 59409516—

反応条件

温度-45 °C

反応手順

A solution of 1-tert-butyl-4-fluoro-benzene (4.54 g, 30 mmol) in THF (100 mL) cooled at −78° C. was treated dropwise with a 2.5M solution of nBuLi in hexane (24 mL, 59 mmol). The reaction mixture was stirred for 5 h at −45° C. then DMF (3.5 mL, 44 mmol) was added at −75° C. and the reaction mixture was stirred for 0.5 h at −75° C. The reaction mixture was poured onto 1N aq. HCl and extracted with Et2O. Combined organic layers were washed with brine, dried over Na2SO4, filtered and evaporated. The title compound was obtained after chromatographic purification (Combi Flash, 40 g silica gel, hexane to hexane-EtOAc 10:1) as a light yellow oil: TLC (hexane-EtOAc 10:1) Rf=0.48, HPLC RtA=2.10 min; 1H NMR (400 MHz, CDCl3): δ10.36 (s, 1H), 7.85 (dd, 1H), 7.62 (m, 1H), 7.08 (dd, 1H), 1.32 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093406B2
出典データセットuspto-grants-2012_01
ORD IDord-4272a5c506464c4e8293a5d378306f8b
出典メモuspto-grants-2012_01