Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diisopropyl Ether → 5-(p-Tolyl)thianthrenium nonafluorobutanesulfonate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diisopropyl Ether | HCID 7914 | — |
| 반응물 | Trifluoroacetic anhydride | HCID 9845 | — |
| 반응물 | Perfluorobutanesulfonic acid | HCID 67815 | — |
| 반응물 | Thianthrene, 5-oxide | HCID 73220 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 5-(p-Tolyl)thianthrenium nonafluorobutanesulfonate | HCID 23137824 | — |
반응 단계
In 10 ml of toluene was dissolved 2 g of thianthrene-S-oxide and the solution was cooled with ice. Then, 2.8 ml of trifluoroacetic anhydride and 1.2 ml of nonafluorobutanesulfonic acid were added thereto, followed by stirring for one hour. Diisopropyl ether was added thereto and the supernatant solution was removed. The residue was purified by a silica gel column (chloroform/methanol=19/1) to obtain 4.4 g of 5-(p-tolyl)thianthrenium nonafluorobutanesulfonate. 1H-NMR (400 MHz, CDCl3): σ 2.34 (s, 3H), 7.08 (d, 2H), 7.22 (d, 2H), 7.78 (m, 6H), 8.65 (d, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07615330B2 |
| 출처 데이터셋 | uspto-grants-2009_11 |
| ORD ID | ord-fe3cbaa672e540b292fbcce13e566fe5 |
| 출처 메모 | uspto-grants-2009_11 |