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HRID 432910作成日:2026年10月26日

Hexamethylenetetramine → 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzaldehyde

https://huagongshe.com/reaction/432910

反応式

関与物質

役割名称HCID仕込み量
反応物HexamethylenetetramineHCID 4101—
反応物Trifluoroacetic acidHCID 6422—
反応物1,3-Dichloro-2-(4-methoxyphenoxy)-5-nitrobenzeneHCID 9972902—
生成物5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzaldehydeHCID 22344863—

反応条件

温度75 °C

反応手順

To a solution of 3,5-dichloro-4-(4-methoxy-phenoxy)-nitrobenzene (3.14 g, 10.0 mmol) in TFA (30 ml) was added hexamethylenetetramine (2.10 g, 15.0 mmol). The resulting mixture was stirred at 75° C. for 2 h then concentrated to a viscous oil. The residue was taken up in 30 ml H2O and stirred at RT. To this suspension was added sufficient sat'd aqueous NaHCO3 to neutralize the residual TFA and the mixture was then extracted with EtOAc (3×30 ml). The combined EtOAc extracts were washed with sat'd aqueous NaHCO3 (2×30 ml) and dried over Na2SO4. Dried extracts were filtered and concentrated to give the title compound of step A (3.67 g) as a yellow solid. The title product of Step A was used in the next step without further purification. MS (APCl−) Calc.: 341.0, Found: 340.1 (M−1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664291B2
出典データセットuspto-grants-2003_12
ORD IDord-c1bf0682f45747e49ab45e8403f2fcb9
出典メモuspto-grants-2003_12