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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 926033생성일: 2026년 10월 25일

Dimethylformamide → HCID 178495951, 화합물

https://huagongshe.com/reaction/926033

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromoethyl methyl etherHCID 80972—
반응물HCID 178501248HCID 178501248—
용매WaterHCID 962—
생성물HCID 178495951HCID 178495951—

반응 조건

온도60 °C

반응 단계

To a mixture of 1.00 g of 2-(trimethylsilyl)ethyl 3-{[trans-4-(methoxycarbonyl)cyclohexyl]sulfamoyl}benzoate and 10 mL of DMF were added 0.63 g of 2-bromoethylmethyl ether and 0.94 g of potassium carbonate at room temperature, followed by stirring at 60° C. overnight. The reaction mixture was cooled to room temperature, and then water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine in this order, and dried over anhydrous sodium sulfate. The resultant was concentrated under reduced pressure, and to a mixture of the obtained residue and 10 mL of THF was added a solution of TBAF in THF (1.0 M, 4.0 mL), followed by stirring at room temperature for 3 hours. A solution of TBAF in THF (1.0 M, 2.0 mL) was further added thereto, followed by stirring at room temperature for 1.5 hours. The reaction mixture was diluted with ethyl acetate, and then washed with 0.2 M hydrochloric acid, water, and saturated brine in this order. The obtained organic layer was dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to obtain 915 mg of 3-{[trans-4-(methoxycarbonyl)cyclohexyl](2-methoxyethyl)sulfamoyl}benzoic acid as a colorless amorphous solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09284295B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-9415bec7f1bd4c5192f0258b8ed08506
출처 메모uspto-grants-2016_03