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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1110053생성일: 2026년 10월 25일

2,6-Di-tert-butyl-4-methylphenol → 6-Butyl-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine-4(3H)-one

https://huagongshe.com/reaction/1110053

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Di-tert-butyl-4-methylphenolHCID 31404—
반응물Acetamidine monohydrochlorideHCID 67170—
반응물Sodium AcetateHCID 517045—
반응물Ethyl 2-[(4-iodophenyl)methyl]-3-oxoheptanoateHCID 19018799—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물6-Butyl-2-methyl-5-[(4-iodophenyl)methyl]pyrimidine-4(3H)-oneHCID 13601404820%

반응 단계

A solution of 2.46 g (6.33 mmol) ethyl 2-[(4-iodophenyl)methyl]-3-oxoheptanoate, 6.0 g (63.3 mmol) acetamidine hydrochloride, 5.2 g (63.3 mmol) sodium acetate, and 84 mg (0.381 mmol) 2,6-di-tert-butyl-4-methylphenol in 30 mL DMF was heated to 153° C. for 12 hours. The cooled reaction mixture was poured into brine and extracted 3 times with ether. The combined organic material was washed with brine, dried over MgSO4, stripped of solvent in vacuo, then was medium pressure chromatographed on silica gel using 1/65/34 AcOH/EtOAc/hexane to give 485 mg of the title compound, 20% yield. Unreacted ethyl 2-[(4-iodophenyl)methyl]-3-oxoheptanoate was recycled. Rf 0.25 in 1/65/34 AcOH/EtOAc/hexane, visualized by UV and ninhydrin stain; 1H-NMR (300 MHz, CDCl3): δ 7.56 (m, 2H), 6.98 (m, 2H), 3.83 (s, 2H), 2.54 (3 line m, 2H), 2.38 (s, 3H), 1.52 (m, 2H), 1.43 (m, 2H), 0.89 (3 line m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05324729
출처 데이터셋uspto-grants-1994_06
ORD IDord-c97c102d53e24eb5a80f80745b9a8d02
출처 메모uspto-grants-1994_06