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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358097생성일: 2026년 10월 24일

Dimethylformamide → 3-Carboethoxymethyl-5-benzylidenerhodanine

https://huagongshe.com/ko/reaction/358097

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ethyl BromideHCID 6332—
반응물Tetramethylammonium hydroxideHCID 60966—
반응물(5-Benzylidene-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)acetic acidHCID 2769989—
용매MethanolHCID 887—
생성물3-Carboethoxymethyl-5-benzylidenerhodanineHCID 4340462—

반응 단계

Under an atmosphere of nitrogen, 4.2 ml of anhydrous N,N-dimethylformamide was added dropwise to 0.279 g of 3-carboxymethyl-5-benzylidenerhodanine (prepared as described in Example 1) at room temperature, and then 1.14 ml of methanol solution of 91.15 mg of tetramethylammonium hydroxide was added dropwise. After the mixture was stirred at room temperature for 20-30 minutes, 0.075 ml of ethyl bromide was added dropwise to the reaction mixture. The mixture was stirred at the same temperature for about 2 hours, and then concentrated under reduced pressure. The residue was diluted with 15 ml of water and extracted with ethyl acetate. The extract was washed with 50 ml of aqueous solution of sodium bicarbonate, 50 ml of water and 50 ml of aqueous solution of sodium chloride, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was recrystallized from a mixture of ethyl acetate and n-hexane (1:3) to obtain 14 mg of the titled compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04464382
출처 데이터셋uspto-grants-1984_08
ORD IDord-515fe300fabe4282982376ddf3db2edc
출처 메모uspto-grants-1984_08