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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1082000생성일: 2026년 10월 25일

2-Methyl-2-butanol → HCID 178463135, 화합물

https://huagongshe.com/reaction/1082000

반응식

참여 물질

역할이름HCID투입량
반응물2-Methyl-2-butanolHCID 6405—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물Potassium CarbonateHCID 11430—
반응물8-Fluoro-4-methoxy-2,5-dimethylthiochroman-6-carboxylic acid-1,1-dioxideHCID 15278521—
반응물HCID 178418331HCID 178418331—
생성물HCID 178463135HCID 17846313576.8%

반응 단계

In a 50-ml flask, 0.70 g (0.0023 mol) of 8-fluoro-4-methoxy-2,5-dimethylthiochroman-6-carboxylic acid-1,1-dioxide, 0.28 g (0.0025 mol) of 1-ethyl-5-hydroxypyrazole and 0.52 g (0.0025 mol) of DCC (N,N'-dicyclohexylcarbodiimide) were added to 5 ml of tert-amyl alcohol at the same time, and the mixture was stirred at room temperature for 30 minutes. Then, 0.17 g (0.00125 mol) of anhydrous potassium carbonate was added. The reaction mixture was allowed to react at 80° C. for 8 hours, and then the reaction solvent was distilled off under reduced pressure. The remainder was dispersed in a 2% potassium carbonate aqueous solution and ethyl acetate to separate it into two phases. Further, the aqueous phase was acidified with 5% hydrochloric acid. and the precipitated oil was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to give 0.70 g of 8-fluoro-4-methoxy-2,5-dimethyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound 40) shown in Table 5. The yield thereof was 78%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05587484
출처 데이터셋uspto-grants-1996_12
ORD IDord-d27bedaecb224c1384119b44b88346d0
출처 메모uspto-grants-1996_12