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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 485113생성일: 2026년 10월 25일

Pyridine → 3-[3,4-dichloro-2(5H)-furanon-5-yl]oxy-3-(2-methyl-4-diethylaminophenyl)phthalide

https://huagongshe.com/reaction/485113

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Thionyl ChlorideHCID 24386—
반응물2-(4-(Diethylamino)-2-methylbenzoyl)benzoic acidHCID 104335—
반응물Mucochloric AcidHCID 2771871—
용매1,2-DichloroethaneHCID 11—
생성물3-[3,4-dichloro-2(5H)-furanon-5-yl]oxy-3-(2-methyl-4-diethylaminophenyl)phthalideHCID 1393150184.2%

반응 단계

In a manner similar to that described in Example 1 above, 2.0 g of 2-(2-methyl-4-diethylaminophenyl)carbonylbenzoic acid, 0.77 g of thionyl chloride and 1.1 g of mucochloric acid were interacted in 20.0 ml of ethylene dichloride in the presence of 0.8 ml of pyridine to obtain 2.5 g of 3-[3,4-dichloro-2(5H)-furanon-5-yl]oxy-3-(2-methyl-4-diethylaminophenyl)phthalide (Formula II: R0 =R=R1 =R2 =H; R4 =R4' =R5 =CH3 ; X=O; Y=3,4-dichloro-2-(5H)-furanon-5-yl), an orange-colored oil. A significant infrared maximum appeared at 1758 cm-1 (C=O;s). A toluene solution of the product spotted on an acidic clay-coated paper developed a yellow-colored image.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04535172
출처 데이터셋uspto-grants-1985_08
ORD IDord-ddc8f338bd104994929db60da594bef1
출처 메모uspto-grants-1985_08