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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1025421생성일: 2026년 10월 23일

Hydrochloric Acid → HCID 178464526, 화합물

https://huagongshe.com/ko/reaction/1025421

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodoethaneHCID 6340—
반응물Potassium CarbonateHCID 11430—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물HCID 178501248HCID 178501248—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물HCID 178464526HCID 178464526—

반응 조건

온도65 °C

반응 단계

A mixture of 450 mg of 2-(trimethylsilyl)ethyl 3-{[trans-4-(methoxycarbonyl)cyclohexyl]sulfamoyl}benzoate, 0.15 mL of ethyl iodide, 422 mg of potassium carbonate, and 4.5 mL of DMF was stirred at 65° C. overnight. To the reaction mixture was added water, followed by extraction with ethyl acetate. Then, the organic layer was washed with water and saturated brine in this order, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to obtain a colorless oily substance. To the obtained oily substance were added a solution of tetrabutyl ammonium fluoride (TBAF) in THF (1.0 M, 2.0 mL) and 4.5 mL of THF, followed by stirring at room temperature for 2 hours. To the reaction mixture was added 0.2 M hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was washed with 0.2 M hydrochloric acid, water, and saturated brine in this order, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to obtain 355 mg of 3-{ethyl[trans-4-(methoxycarbonyl)cyclohexyl]sulfamoyl}benzoic acid as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729068B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-4431d85e244d4e49a8c0b96a036189ad
출처 메모uspto-grants-2014_05