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HRID 324111作成日:2026年10月26日

Phenylboronic Acid → 3,5-Diphenyl-4-[(2-methoxyethoxy)methoxy]-benzaldehyde

https://huagongshe.com/reaction/324111

反応式

関与物質

役割名称HCID仕込み量
反応物Phenylboronic AcidHCID 66827—
反応物3,5-Diiodo-4-(2-methoxyethoxymethoxy)benzaldehydeHCID 22237656—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物3,5-Diphenyl-4-[(2-methoxyethoxy)methoxy]-benzaldehydeHCID 22237509155.5%

反応手順

A mixture of 3,5-diiodo-4-(2-methoxyethoxymethyloxy)-benzaldehyde (19.094 g, 41.327 mmol), Pd(OAc)2(0.185 g, 0.02 mmol), phenylboronic acid (11.429 g, 90.920 mmol) and Ba(OH)2-8H2O (39.114 g, 123.981 mmol) in DME (700 ml) and water (110 ml) was refluxed. After 90 minutes, the reaction mixture was cooled, concentrated to about 400 ml and the residue extracted with EtOAc (1×300 ml, 3×100 ml). The combined organics were washed with saturated NaHCO3 (3×75 ml), water (2×75 ml), brine (2×75 ml), dried over Na2SO4, filtered and the filtrate concentrated in vac and dried. The residue was purified by flash chromatography (hexane, 5% and 12% EtOAc/Hex) to give the product as a light yellow viscous oil (11.645 g, 78%); 1H NMR (400 MHz, DMSO-d6) δ2.79-2.82 (m, 2H), 2.89-2.92 (m, 2H), 3.02 (s, 3H), 4.42 (s, 2H), 7.42-7.46 (m, 2H), 7.48-7.54 (m, 4H), 7.62-7.66 (m, 4H), 7.91 (s, 2H), 10.07 (s, 1H); IR (film) 3050, 2880, 1690,1580 cm−1; mass spectrum [EI], m/z 362 M+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06214877B1
出典データセットuspto-grants-2001_04
ORD IDord-2eeec29e2f884b189580f813d2b7e05a
出典メモuspto-grants-2001_04