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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29249생성일: 2026년 10월 23일

Dichloromethane → 2-(2,4-Dichlorobenzyl-3-methyl-1benzofuran-6-yl]benzamide

https://huagongshe.com/ko/reaction/29249

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sodium CarbonateHCID 10340—
반응물3-BromobenzamideHCID 89807—
반응물HCID 59788883HCID 59788883—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물2-(2,4-Dichlorobenzyl-3-methyl-1benzofuran-6-yl]benzamideHCID 8660740943.8%

반응 단계

To a solution of (2,4-dichlorophenyl)-[3-methyl-6-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-benzofuran-2-yl]-methanone (100 mg, 0.23 mmol) in toluene (4 mL) and ethanol (4 mL) was added 3-bromobenzamide (56 mg, 0.28 mmol) followed by [1,1′-bis(diphenylphosphino)ferrocene]dichloro-palladium (II), complex with dichloromethane (1:1) (17 mg, 0.02 mmol) and 2M aqueous Na2CO3 (0.29 mL, 0.58 mmol). The mixture was degassed under vacuum, then heated to 85 C for 2 h. The reaction mixture was concentrated in vacuo, diluted in methanol, and filtered through a syringe filter. Purification by prep-HPLC provided the desired material as a white solid (41.3 mg, 42%). 1H-NMR (CDCl3) δ 8.02 (t, J=1.9 Hz, 1H), 7.71-7.67 (m, 3H), 7.61 (m, 1H), 7.52 (dd, J=1.4, 8.4 Hz, 1H), 7.46 (t, J=7.7 Hz, 1H), 7.43 (d, J=2.0 Hz, 1H), 7.39 (m, 1H), 7.31 (ddd, J=8.1, 1.9, 0.2 Hz, 1H), 2.54 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420066B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-fa709c035eeb4258bf3f4196f56c05f8
출처 메모uspto-grants-2008_09