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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 917358생성일: 2026년 10월 26일

Sodium Bicarbonate → 6,6-Difluoro-5-methyl-5-hexenyl benzo[1,2,5]thiadiazole-5-carboxylate

https://huagongshe.com/reaction/917358

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물2,1,3-Benzothiadiazole-5-carboxylic acidHCID 602011—
반응물6,6-Difluoro-5-methyl-5-hexenyl methanesulfonateHCID 23020371—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물6,6-Difluoro-5-methyl-5-hexenyl benzo[1,2,5]thiadiazole-5-carboxylateHCID 6918092764%

반응 조건

온도100 °C

반응 단계

To 30 ml of ethanol was dissolved 2.0 g (10 mmol) of methyl benzo[1,2,5]thiadiazole-5-carboxylate, followed by the addition of 3.3 g of a 25% aqueous solution of sodium hydroxide and stirring at room temperature for 3 hours. To the reaction liquid was added 50 ml of water and a dilute hydrochloric acid to make pH of 2. Crystal precipitated was filtered off and dried under reduced pressure to obtain 1.7 g (yield: 92%) of benzo[1,2, 5]thiadiazole-5-carboxylic acid. In a separate reactor, 0.50 g (2.2 mmol) of 6,6-difluoro-5-methyl-5-hexenyl methanesulfonate and 0.43 g (2.4 mmol) of benzo[1,2,5]thiadiazole-5-carboxylic acid were dissolved in 7 ml of N,N-dimethylformamide, followed by the addition of 0.37 g (4.4 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 3 hours. The reaction liquid was then poured in water and extracted with ethyl acetate. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue was purified with silica gel column chromatography (ethyl acetate:hexane=1:19) to obtain 0.44 g (yield: 64%) of 6,6-difluoro-5-methyl-5-hexenyl benzo[1,2,5]thiadiazole-5-carboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07273878B2
출처 데이터셋uspto-grants-2007_09
ORD IDord-2677bad272544f568cd6e7a59e95e6c1
출처 메모uspto-grants-2007_09