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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257984생성일: 2026년 10월 27일

Water → 1-(1,3-dimethyl-4-(3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoyl)-1H-pyrazol-5-yloxy)ethyl methyl carbonate

https://huagongshe.com/reaction/1257984

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1-Chloroethyl methyl carbonateHCID 13506641—
반응물HCID 178496175HCID 178496175—
촉매Tetrabutylammonium BromideHCID 74236—
용매Methyl Ethyl KetoneHCID 6569—
생성물1-(1,3-dimethyl-4-(3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoyl)-1H-pyrazol-5-yloxy)ethyl methyl carbonateHCID 6688442252.6%

반응 단계

5-Hydroxy-1,3-dimethylpyrazol-4-yl 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)phenyl ketone (300 mg) was dissolved in 2-butanone (10 mL), and potassium carbonate (130 mg) and tetrabutyl ammonium bromide (15 mg) were added. After stirring at room temperature for 10 minutes, 1-chloroethyl methyl carbonate (purity: 85%, 270 mg) was added at room temperature, followed by heating and refluxing for 3 hours. After completion of the reaction, the reaction solution was cooled to room temperature and poured into water and then extracted with ethyl acetate. The organic layer was washed with a 1N hydrochloric solution and a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The obtained residue was purified by column chromatography (n-hexane:ethyl acetate=1:1) to obtain the desired product (200 mg) as slightly yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466089B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-e222511c5c7342a9a53fd44aa05d9c93
출처 메모uspto-grants-2013_06