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HRID 595021作成日:2026年10月24日

Ethyl Acetate → 3-Bromo-2,5-difluorobenzaldehyde

https://huagongshe.com/ja/reaction/595021

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物4-Amino-3-bromo-2,5-difluorobenzaldehydeHCID 14621020—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒Hypophosphoric acidHCID 24536—
生成物3-Bromo-2,5-difluorobenzaldehydeHCID 1462102144.1%

反応手順

4-amino-3-bromo-2,5-difluorobenzaldehyde (3.4 g, 14.3 mmol) was dissolved in acetic acid (18 mL) before addition of hypophosphoric acid (50% in water, 39 mL). A solution of sodium nitrite (1.4 eq, 1.4 g) in water (8 mL) was then added dropwise under ice-cooling. After stirring at rt for 2 h, the reaction mixture was poured onto a mixture ice/water and the aqueous phase extracted with DCM. The combined organic phases were dried over sodium sulfate and evaporated. A column chromatography (0 to 10% ethyl acetate in petroleum ether) afforded 3-bromo-2,5-difluorobenzaldehyde (1.3 g, 6.3 mmol, 44%). 1H NMR (d6-DMSO) δ 10.15-10.12 (m, 1H), 8.13 (ddd, J=8.0, 5.0, 3.0 Hz, 1H), 7.66 (ddd, J=8.0, 5.0, 3.0 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242987B2
出典データセットuspto-grants-2016_01
ORD IDord-d33b94c7759147c1ac79f786402c6809
出典メモuspto-grants-2016_01