関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexamethylenetetramine | HCID 4101 | — |
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 1,3-Dichloro-2-(4-methoxyphenoxy)-5-nitrobenzene | HCID 9972902 | — |
| 生成物 | 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzaldehyde | HCID 22344863 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06664291B2 |
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| 出典データセット | uspto-grants-2003_12 |
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| ORD ID | ord-c1bf0682f45747e49ab45e8403f2fcb9 |
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| 出典メモ | uspto-grants-2003_12 |
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