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HRID 29234作成日:2026年10月26日

Dichloromethane → (2,4-Dichloro-phenyl)(3-methyl-6-m-tolyl-benzofuran-2-yl)methanone

https://huagongshe.com/reaction/29234

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Sodium CarbonateHCID 10340—
反応物3-Tolylboronic acidHCID 2733950—
反応物(6-Bromo-3-methyl-benzofuran-2-yl)(2,4-dichloro-phenyl)methanoneHCID 59788907—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
生成物(2,4-Dichloro-phenyl)(3-methyl-6-m-tolyl-benzofuran-2-yl)methanoneHCID 1128088869.3%

反応条件

温度85 °C

反応手順

A solution of (6-Bromo-3-methyl-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone (50 mg, 0.13 mmol) in toluene (1.5 mL) and ethanol (1.5 mL) was degassed with argon for 15 min. At this time, 3-methyl benzene boronic acid (21.2 mg, 0.16 mmol, 1.2 eq) was added followed by [1,1′-bis(diphenylphosphino)-ferrocene]dichloro-palladium(II), complex with dichloromethane (1:1) (10.6 mg, 0.01 mmol, 0.1 eq) and 2M aqueous Na2CO3 (0.21 mL, 3 eq). The reaction was bubbled with argon for another 5 min and then heated to 85° C. for 4 h. The reaction was diluted with ethyl acetate, washed with water, brine, and dried over sodium sulfate. The solvent was removed at reduced pressure and purified on the pre-HPLC to afford 35.6 mg (69%) of a yellow solid as the product. 1H-NMR (CDCl3): δ 7.72 (d, J=8.0 Hz, 1H), 7.65 (s, 1H), 7.57 (dd, J=1.6, 8.0 Hz, 1H), 7.50 (d, J=1.9 Hz, 1H), 7.58 to 7.53 (m, 4H), 7.33 (t, 1H), 7.18 (d, J=7.2 Hz, 1H), 2.56 (s, 3H), 2.42 (s, 3H); LC-MS (MH+=395/397).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420066B2
出典データセットuspto-grants-2008_09
ORD IDord-9ecc41b22e8544a89f7698225a4656f8
出典メモuspto-grants-2008_09