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HRID 51276생성일: 2026년 10월 24일

Veratrole → 4-(2,3-Dimethoxybenzoyl)pyridine

https://huagongshe.com/ko/reaction/51276

반응식

참여 물질

역할이름HCID투입량
반응물VeratroleHCID 7043—
반응물N-Methoxy-N-methylisonicotinamideHCID 3817473—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-(2,3-Dimethoxybenzoyl)pyridineHCID 42854995.3%

반응 단계

A solution of veratrole (8.04 g, 58.2 mmol) in tetrahydrofuran (50 mL) is treated with BuLi (26 mL, 2.5 M in hexane, 65 mmol) at −70° C. After the addition is complete, the reaction mixture is permitted to warm to room temperature and stirred for 2 hours. The mixture is re-cooled to −70° C. and treated with a solution of N-methyl-N-methoxyisonicotinamide (19) (9.15 g, 55.1 mmol) in tetrahydrofuran (30 mL). The resulting slurry is permitted to slowly warm to room temperature over an hour period. When the reaction mixture reaches 0° C. it becomes homogeneous. After 3 hours at room temperature, the reaction is quenched with 10% AcOH (aqueous, 100 mL). After stirring for 45 minutes, the tetrahydrofuran is removed at reduced pressure and the residue is diluted with toluene (150 mL). After neutralization with NHCO3, the phases are separated and the organic phase is submitted to a normal workup to provide an oil. Kugelrohr distillation provides the title compound (12) as a dark oil (12.77 g, 95% yield); b.p. 130-150° C./0.05 mm Hg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713627B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-efb65e0dcdb64cd6bef4ffed51989e58
출처 메모uspto-grants-2004_03