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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65160생성일: 2026년 10월 23일

Methyl iodide → 3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone

https://huagongshe.com/ko/reaction/65160

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물2,4,6-TrimethylanilineHCID 6913—
반응물3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-thioxo-2(1H)-pyrimidinoneHCID 14096477—
용매TetrahydrofuranHCID 8028—
생성물3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinoneHCID 984353370.9%

반응 단계

To a solution of 3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-thioxo-2(1H)-pyrimidinone (1.51 g) in tetrahydrofuran (150 ml) was added methyl iodide (30 ml) and the mixture was refluxed for 90 minutes. The precipitate was added to 2,4,6-trimethylaniline (6 g) and the mixture was heated at 110°-120° C. for 3 hours. The reaction mixture was washed with a mixture of hexane and diisopropyl ether to remove excess 2,4,6-trimethylaniline. The resulting precipitate was collected by filtration and then dissolved in chloroform. The solution was washed with an aqueous solution of sodium bicarbonate, dried over magnesium sulfate and evaporated under reduced pressure to give crude product, which was purified by silica gel column chromatography to give 3,4-dihydro-6-(3,4-dimethoxyphenyl)-1,3-dimethyl-4-(2,4,6-trimethylphenylimino)-2(1H)-pyrimidinone (1.44 g); mp 68°-70° C. Thus obtained compound was recrystallized from a mixture of methanol and water (5:1) to give the desired compound as crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04612376
출처 데이터셋uspto-grants-1986_09
ORD IDord-539b917369d54db2904995e6563294db
출처 메모uspto-grants-1986_09