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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257992생성일: 2026년 10월 25일

Triethylamine → 5-(Ethylthio)carbonyloxy-1-methylpyrazol-4-yl 3-(methoxy)-2-methyl-4-(methylsulfonyl)phenyl ketone

https://huagongshe.com/reaction/1257992

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물Ethyl chlorothioformateHCID 18056—
반응물HCID 178493950HCID 178493950—
용매TetrahydrofuranHCID 8028—
생성물5-(Ethylthio)carbonyloxy-1-methylpyrazol-4-yl 3-(methoxy)-2-methyl-4-(methylsulfonyl)phenyl ketoneHCID 16126850—

반응 단계

To a solution of 5-hydroxy-1-methylpyrazol-4-yl 3-methoxy-2-methyl-4-(methylsulfonyl)phenyl ketone (100 mg, 0.3 mmol) in dry tetrahydrofuran (5 mL) were added triethylamine (61 mg) and 96% S-ethyl chlorothiolformate (50 mg) at room temperature. After the reaction solution was stirred for 1 hour, 150 mL of ethyl acetate was added. The mixture was washed twice with a saturated brine, the organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1) to obtain the desired product as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466088B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-f6a679cd2faf45e58f27fc7b9858ccc5
출처 메모uspto-grants-2013_06