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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1067생성일: 2026년 10월 23일

Pyrazole → 4-Methoxyimino-5-methyl-6-(1-ethyl-5-phenacyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide

https://huagongshe.com/ko/reaction/1067

반응식

참여 물질

역할이름HCID투입량
반응물PyrazoleHCID 1048—
반응물Phenacyl bromideHCID 6259—
반응물Potassium CarbonateHCID 11430—
반응물HCID 178418231HCID 178418231—
용매AcetoneHCID 180—
생성물4-Methoxyimino-5-methyl-6-(1-ethyl-5-phenacyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxideHCID 8675217052%

반응 단계

0.4 Gram (1.1 mmol) of 4-methoxyimino-5-methyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide corresponding to pyrazole derivative (I-H), 0.23 g (1.2 mmol) of phenacyl bromide corresponding to compound B-A-Hal and 0.15 g of potassium carbonate were added to 10 ml of acetone, and the mixture was stirred under heat for 8 hours. Insolubles were removed by filtration, and then the acetone was distilled off. The residue was dissolved in ethyl acetate, and the mixture was washed with a saturated sodium chloride aqueous solution and dried over sodium sulfate. The ethyl acetate was distilled off under reduced pressure, and the residue was subjected to column chromatography (hexane/ethyl acetate) to give 4-methoxyimino-5-methyl-6-(1-ethyl-5-phenacyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound Ib-2) at a yield of 52%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723408
출처 데이터셋uspto-grants-1998_03
ORD IDord-7676d3f705f64b5888f4950efb2b2f22
출처 메모uspto-grants-1998_03