Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Toluenesulfonyl chloride → 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1,3-Diiodopropane | HCID 12314 | — |
| 반응물 | 1,4,7-Triazacyclononane | HCID 188318 | — |
| 반응물 | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 4,7-Bis(p-tolylsulphonyl)-1,4,7-triazacyclononane | HCID 10906262 | — |
| 생성물 | HCID 17939386 | HCID 17939386 | — |
반응 단계
N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) was prepared by reacting (1.1.3) with two equivalents of p-toluenesulfonyl chloride. Two equivalents of N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) hydrobromide were reacted with one equivalent of 1,3-diiodopropane in acetonitrile with excess potassium carbonate. 1,3-bis[N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane propane (1.1.21) was isolated and purified by chromatography. The p-toluene-sulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19). 1.1.22 1,4,7,10-Tetraazabicyclo[5.5.2]tetradecane
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06881732B2 |
| 출처 데이터셋 | uspto-grants-2005_04 |
| ORD ID | ord-40ea47cb16174880a641f1495dd0ae66 |
| 출처 메모 | uspto-grants-2005_04 |