Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 654016생성일: 2026년 10월 25일
Triethylamine → 3-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide]
https://huagongshe.com/reaction/654016
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | alpha-(Aminomethyl)-2,2-dimethyl-1,3-dioxolane-4-methanol | HCID 11971028 | — |
| 반응물 | 3-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid | HCID 15057614 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 3-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-ethylamide] | HCID 15057615 | — |
반응 단계
3.63 g (10 mmol) of 3-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzoic acid is suspended in 36 ml of ethyl acetate, 2.38 g (20 mmol) of thionylchloride is added and the suspension is heated to boiling temperature. After 15 minutes, a clear solution is present, after 1 hour the formation of the acid chloride is complete. The solution is evaporated to dryness under reduce pressure, the residue is concentrated by evaporation in a vacuum twice with 50 ml of dichloromethane each and then dissolved in 36 ml of dioxane. 1.21 g (12 mmol) of triethylamine and 1.93 g (12 mmol) of 2-hydroxy-2-(2,2-dimethyl-I,3-dioxolan-4-yl)-ethylamine are added to this solution and it is stirred for 5 hours at room temperature. The reaction mixture is then evaporated to dryness in a vacuum, the residue is extracted with ethyl acetate, the ethyl acetate extract is concentrated by evaporation in a vacuum and the residue is chromatographed on silica gel 60 (Merck) with ethyl acetate/hexane. 3.42 g (6.75 mmol) =67.5% of the theoretical yield of the product is obtained as an amorphous solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05130119 |
|---|
| 출처 데이터셋 | uspto-grants-1992_07 |
|---|
| ORD ID | ord-c7cb55b0a3ff4b12951c5014a976409f |
|---|
| 출처 메모 | uspto-grants-1992_07 |
|---|