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HRID 29656作成日:2026年10月24日

4-Phenylbenzoyl chloride → 2-(4-phenylbenzoyl)oxy-4-[2-[(E)-1-phenylethylideneamino]oxyethoxy]benzoic acid

https://huagongshe.com/ja/reaction/29656

反応式

関与物質

役割名称HCID仕込み量
反応物4-Phenylbenzoyl chlorideHCID 84151—
反応物2-Hydroxy-4-[2-({[1-phenylethylidene]amino}oxy)ethoxy]benzoic acidHCID 86039301—
生成物2-(4-phenylbenzoyl)oxy-4-[2-[(E)-1-phenylethylideneamino]oxyethoxy]benzoic acidHCID 87734387—

反応手順

The title compound was prepared as a white solid (0.076 g, 40%) from 2-hydroxy-4-[2-({[1-phenylethylidene]amino}oxy)ethoxy]benzoic acid and biphenyl-4-carbonyl chloride using a procedure similar to example 8. mp=157.5-159.1° C.; mass spectrum (+EI, M+) m/z 495. 1H NMR (400 MHz, DMSO-d6); δ 12.67 (s, 1H), 8.14 (d, 2H), 7.93 (d, 1H), 7.88 (d, 1H), 7.78 (d, 2H), 7.65 (dd, 2H), 7.52 (dd, 2H), 7.45 (dd, 1H), 7.38 (s, 1H), 7.36 (d, 2H), 7.04 (dd, 1H), 7.02 (s, 1H), 4.47(t, 2H), 4.40 (t, 2H), 2.17 (s, 3H). Elemental analysis: Calcd. for C30H25NO6: C, 70.72H, 5.09; N, 2.83, Found: C, 70.92; H, 4.92; N, 2.76.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420083B2
出典データセットuspto-grants-2008_09
ORD IDord-50f8cff905c74100bc7135b77ab93b73
出典メモuspto-grants-2008_09