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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4444생성일: 2026년 10월 23일

Acetic Acid → 3-Hydroxymethyl-5-dichloromethyl-2-phthalimidopyrazine

https://huagongshe.com/ko/reaction/4444

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물DichloromethaneHCID 6344—
반응물Potassium AcetateHCID 517044—
반응물3-Chloromethyl-5-dichloromethyl-2-phthalimidopyrazineHCID 13604769—
용매(Methanesulfinyl)methane--water (1/1)HCID 23503278—
생성물3-Hydroxymethyl-5-dichloromethyl-2-phthalimidopyrazineHCID 1360477747%

반응 단계

50 ml of glacial acetic acid and 35 g of potassium acetate were added to a solution of 57.7 g (0.16 mole) of 65% strength 3-chloromethyl-5-dichloromethyl-2-phthalimidopyrazine in 1,000 ml of a 95:5 dimethyl sulfoxide/water mixture. The mixture was stirred for three days at room temperature, after which 1,000 ml of dichloromethane and 1,000 ml of ice-water were added, the resulting mixture was mixed thoroughly and phase separation was effected. The aqueous phase was washed once with 500 ml of dichloromethane and once with 250 ml of dichloromethane, and the combined organic phases were washed twice with 1,000 ml of water, dried over sodium sulfate and evaporated down. The resulting black oil was brought to crystallization with 50 ml of methanol, and then recrystallized from 700 ml of methanol. 16.6 g (47%) of 5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine of melting point 191°-192° C. (sublimation with decomposition) were obtained. 1H-NMR (200 MHz, CDCl3): δ3.3 (t, OH), 4.8 (d, 2H), 6.9 (s, 1H), 8.0 (m, 4H), 9.1 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04725689
출처 데이터셋uspto-grants-1988_02
ORD IDord-e68e567d6ece4a128886cf5a849df771
출처 메모uspto-grants-1988_02