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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 867607생성일: 2026년 10월 24일

Sulfuric Acid → 4-Amino-3,5-dimethoxybenzaldehyde

https://huagongshe.com/ko/reaction/867607

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물5-(4-Amino-3,5-dimethoxyphenyl)-5-hydroxybarbituric acidHCID 21290280—
용매WaterHCID 962—
생성물4-Amino-3,5-dimethoxybenzaldehydeHCID 20042963—

반응 단계

28 ml of sulfuric acid (d=1.8; 0.45 mol) were heated to 120° while stirring and treated in one portion with 11.25 g of 5-(4-amino-3,5-dimethoxyphenyl)-5-hydroxybarbituric acid (0.038 mol). The mixture was stirred until evolution of gas was no longer observed (about 15-20 minutes) and then poured into a mixture of 140 g of ice and 140 g of water while stirring. Resinous polymerization products were separated by a filtration over a pad of 15 g of celite. While stirring and cooling, the filtrate was treated with 63.6 g of potassium carbonate powder until neutral. The aqueous suspension was extracted three times with 50 ml of ethyl acetate each time, the combined organic phases were dried over sodium sulfate and concentrated in water-jet vacuum. The residue was dried up to constant weight in a high vacuum. There was obtained 6.36 of crude 4-amino-3,5-dimethoxybenzaldehyde as a yellow oil which solidified on standing (mp=94°-96° C.). The purity determined by gas chromatography was 96%. 4-amino-3,5-dimethoxybenzaldehyde was converted into 2,4diamino-5-(4-amino-3,5-dimethoxybenzyl)pyrimidine as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04775756
출처 데이터셋uspto-grants-1988_10
ORD IDord-608b0e4ca43044a39a3be6b4e069cdc3
출처 메모uspto-grants-1988_10