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HRID 1992932作成日:2026年10月25日

Cesium carbonate → 4-({3-Butyl-2-[4-(methyloxy)phenyl]-1-naphthalenyl}oxy)benzaldehyde

https://huagongshe.com/reaction/1992932

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-FluorobenzaldehydeHCID 68023—
反応物3-Butyl-2-[4-(methyloxy)phenyl]-1-naphthalenolHCID 68537410—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-({3-Butyl-2-[4-(methyloxy)phenyl]-1-naphthalenyl}oxy)benzaldehydeHCID 8608711569%

反応手順

3-Butyl-2-[4-(methyloxy)phenyl]-1-naphthalenol (160) (0.25 g, 0.82 mmol) and 4-fluorobenzaldehyde was heated with Cs2CO3 in DMSO at 100° C. to give 0.23 g (69%) of compound 161 as a light brown viscous oil. 1H NMR (400 MHz, CDCl3): δ 0.80 (t, J=7.3 Hz, 3H), 1.20-1.30 (m, 2H), 1.40-1.50 (m, 2H), 2.60 (t, J=7.8 Hz, 2H), 3.78 (s, 3H), 6.71 (d, J=8.8 Hz, 2H), 6.79 (d, J=8.6 Hz, 2H), 7.05 (d, J=8.7 Hz, 2H), 7.39 (t, J=7.4 Hz, 1H), 7.50 (t, J=7.5 Hz, 1H), 7.64 (d, J=8.8 Hz, 2H), 7.70 (s, 1H), 7.77 (d, J=8.2 Hz, 1H), 7.87 (d, J=8.1 Hz, 1H), 9.81 (s, 1H). LCMS (ESI): m/z 411 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07649093B2
出典データセットuspto-grants-2010_01
ORD IDord-cf59c30338ff48c3bbc0dedded3492cb
出典メモuspto-grants-2010_01