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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2209464생성일: 2026년 10월 27일

Methanol → HCID 54509567, 화합물

https://huagongshe.com/reaction/2209464

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물3-Nitrophenylboronic AcidHCID 1677—
반응물Sodium CarbonateHCID 10340—
반응물2-bromo-4-(4-pyridinylmethyl)BenzenamineHCID 21865645—
용매BenzeneHCID 241—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
용매AluminumHCID 5359268—
생성물HCID 54509567HCID 5450956785.3%

반응 단계

4-(4-Amino-3-bromobenzyl)pyridine (1.0 gm), 3-nitrobenzene boronic acid (0.63 gm), palladium tetrakis triphenylphosphine (0.47 gm), methanol (6.5 mL), 2.0M Na2CO3 (1.9 mL) and benzene (32 mL) are combined in a reaction flask that is wrapped in aluminum foil (to prevent exposure of the reagents to light). The reaction mixture is heated to reflux for 6 hours. The progress of the reaction is monitored by thin-layer chromatography (9:1 hexane:ethyl acetate). When the starting material is converted, the reaction mixture is allowed to cool and the solvents are removed. Ethyl acetate is added to the residue, the resultant solution is filtered through a pad of Na2SO4, and concentrated. The product is isolated by preparative thin-layer chromatography (9:1 hexane:ethyl acetate) yielding 983 mg of 4-[4-amino-3-(3-nitrophenyl)benzyl]pyridine as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05455252
출처 데이터셋uspto-grants-1995_10
ORD IDord-81a3102cb48e4c0b8237898f90eb372f
출처 메모uspto-grants-1995_10